Introduction to Whole Gene
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Whole Gene sentence examples within next generation sequencing
A next-generation sequencing (NGS) workflow based on whole gene sequencing of BAG3, DSP, FLNC, and LMNA of a cohort of 95 DCM patients, for whom no putatively causative point mutations were identified after NGS of a panel of 48 cardiomyopathy-causing genes, was thus performed.
A next-generation sequencing (NGS) workflow based on whole gene sequencing of BAG3, DSP, FLNC, and LMNA of a cohort of 95 DCM patients, for whom no putatively causative point mutations were identified after NGS of a panel of 48 cardiomyopathy-causing genes, was thus performed.
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Current approaches to characterize the mutational profile of CFTR are based on targeted mutation analysis (TMA) or whole gene studies derived from short-read next generation sequencing (NGS).
Current approaches to characterize the mutational profile of CFTR are based on targeted mutation analysis (TMA) or whole gene studies derived from short-read next generation sequencing (NGS).
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Whole Gene sentence examples within Heterozygou Whole Gene
The genetic analysis revealed 20 RB1 variations in 29 probands, inclusive of 3 novel mutations, known 16 mutations and heterozygous whole gene deletions.
The genetic analysis revealed 20 RB1 variations in 29 probands, inclusive of 3 novel mutations, known 16 mutations and heterozygous whole gene deletions.
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The genetic analysis revealed 20 RB1 variations in 29 probands (79%), inclusive of 3 novel mutations, previously reported 16 mutations and heterozygous whole gene deletions.
The genetic analysis revealed 20 RB1 variations in 29 probands (79%), inclusive of 3 novel mutations, previously reported 16 mutations and heterozygous whole gene deletions.
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Whole Gene sentence examples within Detected Whole Gene
In addition, we detected whole gene expression profiling between primary tumors and PDX generations.
In addition, we detected whole gene expression profiling between primary tumors and PDX generations.
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We have detected whole gene level deletion/duplication, single/multi exonic level deletion/duplication, partial exonic deletion and mosaic deletion.
We have detected whole gene level deletion/duplication, single/multi exonic level deletion/duplication, partial exonic deletion and mosaic deletion.
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Whole Gene sentence examples within whole gene deletion
After excluding 2 MGIT-BDQ-resistant isolates with borderline resistance (GU400growth control-GU100BDQ≤1day), 100% (15/15) harbored Rv0678 gene mutations, including seven novel mutations [g-14a, Ile80Ser (N=2), Phe100Tyr, Ala102Val, Ins g 181–182 frameshift mutation (N=2), Del 11–63 frameshift mutation, and whole gene deletion (N=2)].
After excluding 2 MGIT-BDQ-resistant isolates with borderline resistance (GU400growth control-GU100BDQ≤1day), 100% (15/15) harbored Rv0678 gene mutations, including seven novel mutations [g-14a, Ile80Ser (N=2), Phe100Tyr, Ala102Val, Ins g 181–182 frameshift mutation (N=2), Del 11–63 frameshift mutation, and whole gene deletion (N=2)].
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Whole Gene sentence examples within whole gene expression
Whole Gene sentence examples within whole gene sequencing
The whole gene sequencing results showed that Case C, Case D, and Case E added a common mutation site (C27092T) based on the sequence of Case A, and Case B possessed a new mutation site (T21673C) compared with Case A’s sequence.
The whole gene sequencing results showed that Case C, Case D, and Case E added a common mutation site (C27092T) based on the sequence of Case A, and Case B possessed a new mutation site (T21673C) compared with Case A’s sequence.
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A next-generation sequencing (NGS) workflow based on whole gene sequencing of BAG3, DSP, FLNC, and LMNA of a cohort of 95 DCM patients, for whom no putatively causative point mutations were identified after NGS of a panel of 48 cardiomyopathy-causing genes, was thus performed.
A next-generation sequencing (NGS) workflow based on whole gene sequencing of BAG3, DSP, FLNC, and LMNA of a cohort of 95 DCM patients, for whom no putatively causative point mutations were identified after NGS of a panel of 48 cardiomyopathy-causing genes, was thus performed.
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Whole Gene sentence examples within whole gene sequence
The mutants of each isoform among tested rice varieties were identified by amino-acid mutations in coding sequences based on the extraction and analysis of whole gene sequences.
The mutants of each isoform among tested rice varieties were identified by amino-acid mutations in coding sequences based on the extraction and analysis of whole gene sequences.
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Then, the product was purified and sequenced to acquire the whole gene sequence of the N protein and its encoded amino acid sequence.
Then, the product was purified and sequenced to acquire the whole gene sequence of the N protein and its encoded amino acid sequence.
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Whole Gene sentence examples within whole gene level
We have detected whole gene level deletion/duplication, single/multi exonic level deletion/duplication, partial exonic deletion and mosaic deletion.
We have detected whole gene level deletion/duplication, single/multi exonic level deletion/duplication, partial exonic deletion and mosaic deletion.
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Alternative splicing and polyadenylation play a crucial role in the functional diversity of a gene by generating different isoforms to regulate gene expression at the post-transcriptional level, and limiting analyses to the whole gene level can miss this important regulatory layer.
Alternative splicing and polyadenylation play a crucial role in the functional diversity of a gene by generating different isoforms to regulate gene expression at the post-transcriptional level, and limiting analyses to the whole gene level can miss this important regulatory layer.
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Whole Gene sentence examples within whole gene duplication
By examining the biosynthesis of the anti-tubercular wollamides, we show how whole gene duplication and neofunctionalization can result in pathway bifurcation.
By examining the biosynthesis of the anti-tubercular wollamides, we show how whole gene duplication and neofunctionalization can result in pathway bifurcation.
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We noted some order-specific trends in oskar sequence evolution, including whole gene duplications, clade-specific losses, and rapid divergence.
We noted some order-specific trends in oskar sequence evolution, including whole gene duplications, clade-specific losses, and rapid divergence.
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Whole Gene sentence examples within whole gene length
Whole Gene sentence examples within whole gene family
Conclusion This study reports the first association of inherited CEACAM mutations and breast cancer risk, and potentially implicates the whole gene family in genetic risk.
Conclusion This study reports the first association of inherited CEACAM mutations and breast cancer risk, and potentially implicates the whole gene family in genetic risk.
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To evaluate the combined contribution of the whole gene family, we constructed a ripS-null mutant of strain OE1-1 of R.
To evaluate the combined contribution of the whole gene family, we constructed a ripS-null mutant of strain OE1-1 of R.
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Whole Gene sentence examples within whole gene structure
Deciphering this regulatory code, and how the whole gene structure interacts to produce mRNA transcripts and regulate mRNA abundance, can greatly improve our capabilities for controlling gene expression.
Deciphering this regulatory code, and how the whole gene structure interacts to produce mRNA transcripts and regulate mRNA abundance, can greatly improve our capabilities for controlling gene expression.
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The phasing of Iso-Seq data provided a great advantage in separating the whole gene structure and producing a significantly higher separation ratio than RNA-Seq.
The phasing of Iso-Seq data provided a great advantage in separating the whole gene structure and producing a significantly higher separation ratio than RNA-Seq.
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10.1177/02698811211003495
It is generally unknown by whole generations of psychiatrists that the classical psychedelics d-lysergic acid diethylamide (LSD) and psilocybin were prescribable medicines in psychiatry throughout the USA and Europe until prohibition was effectively imposed on routine clinical use and most scientific research around 1970.
It is generally unknown by whole generations of psychiatrists that the classical psychedelics d-lysergic acid diethylamide (LSD) and psilocybin were prescribable medicines in psychiatry throughout the USA and Europe until prohibition was effectively imposed on routine clinical use and most scientific research around 1970.
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10.3390/genes12030364
The genotype–phenotype correlation is not fully understood, but it has been hypothesised that type I BPES involves more severe loss of function variants spanning the whole gene.
The genotype–phenotype correlation is not fully understood, but it has been hypothesised that type I BPES involves more severe loss of function variants spanning the whole gene.
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10.3389/fonc.2021.726551
Methods We used the assay for transposase-accessible chromatin with high-throughput sequencing (ATAC-seq) to analyse chromatin accessibility in the promoter regions of whole genes in liver hepatocellular carcinoma (LIHC) and then screened differentially expressed genes (DEGs) at the mRNA level by transcriptome sequencing technology (RNA-seq).
Methods We used the assay for transposase-accessible chromatin with high-throughput sequencing (ATAC-seq) to analyse chromatin accessibility in the promoter regions of whole genes in liver hepatocellular carcinoma (LIHC) and then screened differentially expressed genes (DEGs) at the mRNA level by transcriptome sequencing technology (RNA-seq).
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10.1002/humu.24284
Both the pathogenic and likely pathogenic variants scattered on the whole gene length of DYSF.
Both the pathogenic and likely pathogenic variants scattered on the whole gene length of DYSF.
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10.21203/rs.3.rs-796690/v1
Whole genes of 3kb to 4kb were successfully amplified.
Whole genes of 3kb to 4kb were successfully amplified.
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10.1080/13803395.2021.1912300
Haplotype analyses revealed significant associations between the whole gene and brain phenotypes.
Haplotype analyses revealed significant associations between the whole gene and brain phenotypes.
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10.1097/MD.0000000000026062
This study first identified key lncRNAs, miRNAs and their targets, and further revealed a global view of lncRNA-associated ceRNA network involved in DKD by using whole gene transcripts analysis.
This study first identified key lncRNAs, miRNAs and their targets, and further revealed a global view of lncRNA-associated ceRNA network involved in DKD by using whole gene transcripts analysis.
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10.3389/fmicb.2021.754249
After excluding 2 MGIT-BDQ-resistant isolates with borderline resistance (GU400growth control-GU100BDQ≤1day), 100% (15/15) harbored Rv0678 gene mutations, including seven novel mutations [g-14a, Ile80Ser (N=2), Phe100Tyr, Ala102Val, Ins g 181–182 frameshift mutation (N=2), Del 11–63 frameshift mutation, and whole gene deletion (N=2)].
After excluding 2 MGIT-BDQ-resistant isolates with borderline resistance (GU400growth control-GU100BDQ≤1day), 100% (15/15) harbored Rv0678 gene mutations, including seven novel mutations [g-14a, Ile80Ser (N=2), Phe100Tyr, Ala102Val, Ins g 181–182 frameshift mutation (N=2), Del 11–63 frameshift mutation, and whole gene deletion (N=2)].
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10.3389/fphar.2021.694562
The cytotoxicity to different cancer cell lines was screened using MTT assay and then whole gene expression was elucidated using microarray.
The cytotoxicity to different cancer cell lines was screened using MTT assay and then whole gene expression was elucidated using microarray.
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10.3390/EN14092605
The final goal of the phase change material tank model is to be implemented into the whole generic heating system model.
The final goal of the phase change material tank model is to be implemented into the whole generic heating system model.
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10.1038/s41416-021-01491-x
DISCUSSION
The exploration of the whole gene expression profile characterising aggressive OSCC tumours highlights their enhanced proliferative and poorly differentiated intrinsic nature.
DISCUSSION
The exploration of the whole gene expression profile characterising aggressive OSCC tumours highlights their enhanced proliferative and poorly differentiated intrinsic nature.
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10.1016/j.gene.2021.145543
The study aims to retrospect the association between SNPs of whole genes and AG risk by meta-analysis.
The study aims to retrospect the association between SNPs of whole genes and AG risk by meta-analysis.
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10.1021/acs.biomac.1c00248
The mutants of each isoform among tested rice varieties were identified by amino-acid mutations in coding sequences based on the extraction and analysis of whole gene sequences.
The mutants of each isoform among tested rice varieties were identified by amino-acid mutations in coding sequences based on the extraction and analysis of whole gene sequences.
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10.3390/pharmaceutics13010077
Whole gene expression profiles from total RNA isolated from whole blood samples of six responders and six non-responders taken before administration of the biologic and after two weeks of therapy were analyzed using next-generation RNA sequencing.
Whole gene expression profiles from total RNA isolated from whole blood samples of six responders and six non-responders taken before administration of the biologic and after two weeks of therapy were analyzed using next-generation RNA sequencing.
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10.1101/2021.09.09.459557
To make the whole genetic analysis in animal and plant breeding straightforward, we developed a powerful, robust and fast R package that includes genomic data format conversion, genomic data quality control and genotype imputation, breed composition analysis, pedigree tracing, analysis and visualization, pedigree-based and genomic-based relationship matrix construction, and genomic evaluation.
To make the whole genetic analysis in animal and plant breeding straightforward, we developed a powerful, robust and fast R package that includes genomic data format conversion, genomic data quality control and genotype imputation, breed composition analysis, pedigree tracing, analysis and visualization, pedigree-based and genomic-based relationship matrix construction, and genomic evaluation.
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10.2139/SSRN.3784896
Using a cocktail of four sgRNAs targeting a single genomic region mixed with a marker-sgRNA against the pigmentation gene tyrosinase (tyr), we demonstrate that one can easily and accurately excise genomic regions such as promoters, protein domains, specific exons or whole genes.
Using a cocktail of four sgRNAs targeting a single genomic region mixed with a marker-sgRNA against the pigmentation gene tyrosinase (tyr), we demonstrate that one can easily and accurately excise genomic regions such as promoters, protein domains, specific exons or whole genes.
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10.12688/f1000research.40338.2
Nexus copy number software from BioDiscovery was used for evaluation of copy number variants and whole gene deletions.
Nexus copy number software from BioDiscovery was used for evaluation of copy number variants and whole gene deletions.
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10.21203/rs.3.rs-589027/v1
These studies assign the term “essential” to whole genes rather than the protein domain sequences that confer the essential functions.
These studies assign the term “essential” to whole genes rather than the protein domain sequences that confer the essential functions.
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10.1017/EPI.2020.53
I outline an approach in which we can – in usual cases – reason using conjunctions without accepting the closure in its whole generality.
I outline an approach in which we can – in usual cases – reason using conjunctions without accepting the closure in its whole generality.
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10.46234/ccdcw2021.151
The whole gene sequencing results showed that Case C, Case D, and Case E added a common mutation site (C27092T) based on the sequence of Case A, and Case B possessed a new mutation site (T21673C) compared with Case A’s sequence.
The whole gene sequencing results showed that Case C, Case D, and Case E added a common mutation site (C27092T) based on the sequence of Case A, and Case B possessed a new mutation site (T21673C) compared with Case A’s sequence.
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10.1016/j.aspen.2021.07.004
The survival rates of eggs, larvae and the whole generation were the highest at 26℃, which were 87.
The survival rates of eggs, larvae and the whole generation were the highest at 26℃, which were 87.
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10.1371/journal.pone.0250458
Because GANs are not effective with whole genes, we first selected significant genes using DNA mutation data and random forest feature ranking.
Because GANs are not effective with whole genes, we first selected significant genes using DNA mutation data and random forest feature ranking.
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10.1111/ijlh.13715
Also, we found one suspected case of whole gene deletion.
Also, we found one suspected case of whole gene deletion.
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10.31143/2542-212x-2021-2-154-165
The aim of the study is to recreate a complete biographical and creative picture of the life of a talented writer, philologist, educator, educator who raised a whole generation of artists and workers of culture and education.
The aim of the study is to recreate a complete biographical and creative picture of the life of a talented writer, philologist, educator, educator who raised a whole generation of artists and workers of culture and education.
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10.5772/intechopen.97574
Whole gene deletion in animals does not successfully model the disease, as NF-1 cases caused by point mutations could be differentially affected by cell type-specific alternative splice variants of NF1.
Whole gene deletion in animals does not successfully model the disease, as NF-1 cases caused by point mutations could be differentially affected by cell type-specific alternative splice variants of NF1.
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10.3390/jcm10122710
Results: A total of 117 different ABCC6 rare sequence variants were detected as being spread through the whole gene.
Results: A total of 117 different ABCC6 rare sequence variants were detected as being spread through the whole gene.
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10.1186/s40478-020-01113-2
The panel covers either mutation hotspots or—where loss of function is a known mechanism of action—whole genes.
The panel covers either mutation hotspots or—where loss of function is a known mechanism of action—whole genes.
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10.1177/0020715221992501
Most generalizations take the form of part-whole generalizations, when authors discuss how global forces operated in Brazil and what the case of Brazil can teach us about the global agri-food system under neoliberalism.
Most generalizations take the form of part-whole generalizations, when authors discuss how global forces operated in Brazil and what the case of Brazil can teach us about the global agri-food system under neoliberalism.
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10.3390/ijms22168647
Subsequent analysis of clones showed the distribution of mutations over the whole gene.
Subsequent analysis of clones showed the distribution of mutations over the whole gene.
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10.1016/j.jiac.2021.01.016
METHODS
SN was evaluated against three segments of FKS1 and FKS2 genes including whole gene, regions including all HSs, and the region including only HS1.
METHODS
SN was evaluated against three segments of FKS1 and FKS2 genes including whole gene, regions including all HSs, and the region including only HS1.
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10.1186/s13023-021-01841-1
Unresolved pedigrees underwent further studies (whole gene/whole exome/whole genome sequencing).
Unresolved pedigrees underwent further studies (whole gene/whole exome/whole genome sequencing).
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10.1186/s40814-021-00834-y
The ThinkCancer! workshop is an educational behaviour change intervention aimed at the whole general practice team, designed to improve primary care approaches to ensure timely diagnosis of cancer.
The ThinkCancer! workshop is an educational behaviour change intervention aimed at the whole general practice team, designed to improve primary care approaches to ensure timely diagnosis of cancer.
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10.3389/fgene.2021.702889
Conclusion This study reports the first association of inherited CEACAM mutations and breast cancer risk, and potentially implicates the whole gene family in genetic risk.
Conclusion This study reports the first association of inherited CEACAM mutations and breast cancer risk, and potentially implicates the whole gene family in genetic risk.
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10.1017/pds.2021.495
A big part of the whole general arrangement process is finding an optimized compartment layout.
A big part of the whole general arrangement process is finding an optimized compartment layout.
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10.1158/1538-7445.AM2021-LB047
Duplex sequencing, an ultra-accurate error-correction sequencing approach, was used to deeply sequence extracted DNA from lavage samples (average duplex depth ~2500x) with a panel of candidate ovarian cancer driver genes including TP53, ARID1A, PTEN, PPP2R1A, CDKN2A, KRAS (whole genes), CTNNB1, PIK3CA, and BRAF (hotspots only).
Duplex sequencing, an ultra-accurate error-correction sequencing approach, was used to deeply sequence extracted DNA from lavage samples (average duplex depth ~2500x) with a panel of candidate ovarian cancer driver genes including TP53, ARID1A, PTEN, PPP2R1A, CDKN2A, KRAS (whole genes), CTNNB1, PIK3CA, and BRAF (hotspots only).
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10.1101/2021.07.15.452480
This however limits the size of the designed DNA to span merely a part of a single regulatory region, whereas the whole gene regulatory structure including the coding and adjacent non-coding regions is involved in controlling gene expression.
This however limits the size of the designed DNA to span merely a part of a single regulatory region, whereas the whole gene regulatory structure including the coding and adjacent non-coding regions is involved in controlling gene expression.
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10.12688/F1000RESEARCH.40338.1
Nexus copy number software from BioDiscovery was used for evaluation of copy number variants and whole gene deletions.
Nexus copy number software from BioDiscovery was used for evaluation of copy number variants and whole gene deletions.
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10.1111/cge.14035
Missense, nonsense, frameshift, or intronic rare variants almost complete the characterization afterwhole gene Sanger sequencing, but a small percentage of patients remain uncharacterized.
Missense, nonsense, frameshift, or intronic rare variants almost complete the characterization afterwhole gene Sanger sequencing, but a small percentage of patients remain uncharacterized.
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10.4274/jcrpe.galenos.2021.2021.0128
1528C>T in one allele and a whole gene deletion in the other) with early growth impairment in infancy.
1528C>T in one allele and a whole gene deletion in the other) with early growth impairment in infancy.
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10.11648/J.IJLA.20210904.17
At first they are taken into consideration the scholar's training at the school of Alessandro D’Ancona (1835-1914), who was also an important scholar of popular literature, as well as of Dante, and was able to initiate a whole generation of his pupils to investigate folklore.
At first they are taken into consideration the scholar's training at the school of Alessandro D’Ancona (1835-1914), who was also an important scholar of popular literature, as well as of Dante, and was able to initiate a whole generation of his pupils to investigate folklore.
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10.1186/s12891-020-03924-9
Furthermore, a whole gene chip analysis suggested that the expression levels of CLCF1 in the peripheral blood mononuclear cells (PBMCs) were downregulated in postmenopausal women with osteoporosis.
Furthermore, a whole gene chip analysis suggested that the expression levels of CLCF1 in the peripheral blood mononuclear cells (PBMCs) were downregulated in postmenopausal women with osteoporosis.
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10.1007/s10072-021-05117-1
Since no common mutation in autosomal recessive (AR) cerebellar ataxias, whole gene sequencing provide an advantage to detect novel mutations and may be more effective for clinical diagnosis.
Since no common mutation in autosomal recessive (AR) cerebellar ataxias, whole gene sequencing provide an advantage to detect novel mutations and may be more effective for clinical diagnosis.
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10.1093/labmed/lmaa116
This report emphasizes the benefit of sequencing the whole gene in individuals who are negative for hotspot mutation of achondroplasia with strong clinical suspicion.
This report emphasizes the benefit of sequencing the whole gene in individuals who are negative for hotspot mutation of achondroplasia with strong clinical suspicion.
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10.1002/ajmg.a.62518
Patients with SOX2 nucleotide variants, whole gene deletions or translocations are typically affected with bilateral or unilateral microphthalmia and anophthalmia.
Patients with SOX2 nucleotide variants, whole gene deletions or translocations are typically affected with bilateral or unilateral microphthalmia and anophthalmia.
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10.1002/hast.1216
The Covid‐19 intensification of burnout can serve as a wake‐up call that the structure of health care needs to be improved if we are to prevent the loss of a whole generation of empathic clinicians.
The Covid‐19 intensification of burnout can serve as a wake‐up call that the structure of health care needs to be improved if we are to prevent the loss of a whole generation of empathic clinicians.
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10.2174/1389557521666210913112030
Over the past few decades, the development of CRISPR (clustered regularly interspaced short palindromic repeat) has revolutionized the whole genetic engineering process utilizing the principles of Watson-Crick base pairing.
Over the past few decades, the development of CRISPR (clustered regularly interspaced short palindromic repeat) has revolutionized the whole genetic engineering process utilizing the principles of Watson-Crick base pairing.
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10.21608/JNSBU.2021.159639
Competence of performance is important in education and the whole generation of nurses.
Competence of performance is important in education and the whole generation of nurses.
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10.1016/B978-0-12-821477-0.00014-3
The reduced cost of whole gene synthesis has facilitated the process of making modifications in the genomic structure and function, thereby paving the path for the synthesis of genomes from scratch.
The reduced cost of whole gene synthesis has facilitated the process of making modifications in the genomic structure and function, thereby paving the path for the synthesis of genomes from scratch.
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10.1007/978-3-030-73770-2_17
The ease of uploading images on Instagram has meant that a whole generation grows up paying closer attention to visual language.
The ease of uploading images on Instagram has meant that a whole generation grows up paying closer attention to visual language.
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10.1007/S10032-021-00374-4
This process drives the system to sustain the main structure of the characters throughout the whole generation processes.
This process drives the system to sustain the main structure of the characters throughout the whole generation processes.
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10.1101/2021.06.03.446923
Using 197 of the Drosophila Genetic Reference Panel (DGRP) lines, we surveyed variation across single nucleotide polymorphisms, whole genes, and epistatic interactions to find genetic modifiers robustness for flight performance.
Using 197 of the Drosophila Genetic Reference Panel (DGRP) lines, we surveyed variation across single nucleotide polymorphisms, whole genes, and epistatic interactions to find genetic modifiers robustness for flight performance.
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10.1101/2021.06.03.446321
On the adult slide, 10 clusters were obtained based on whole gene expression similarities.
On the adult slide, 10 clusters were obtained based on whole gene expression similarities.
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10.3748/wjg.v27.i28.4653
However, the genetic variation analysis in these studies is incomplete and isolated, pointing out only a few single nucleotide polymorphisms (SNPs) and the risk of gastric cancer, and no comprehensive study covering the whole gene region has been carried out.
However, the genetic variation analysis in these studies is incomplete and isolated, pointing out only a few single nucleotide polymorphisms (SNPs) and the risk of gastric cancer, and no comprehensive study covering the whole gene region has been carried out.
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10.1038/s41598-021-96078-0
However, no chronological assessment of whole gene expression profiles has been conducted.
However, no chronological assessment of whole gene expression profiles has been conducted.
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10.1210/jendso/bvab048.256
Due to sporadic follow-up, their diagnosis and care were delayed until age 15y when AD was confirmed with genetic testing (compound heterozygous: whole gene deletion on one allele and c.
Due to sporadic follow-up, their diagnosis and care were delayed until age 15y when AD was confirmed with genetic testing (compound heterozygous: whole gene deletion on one allele and c.
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10.1504/ijguc.2021.10034612
The quality of the proposed methodology is tried and approved on the standard IEEE 3, 6 and the 10-unit systems by solving some cases as the fuel cost minimisation, whole generation cost minimisation, emission minimisation, and at the same time the system transmission loss.
The quality of the proposed methodology is tried and approved on the standard IEEE 3, 6 and the 10-unit systems by solving some cases as the fuel cost minimisation, whole generation cost minimisation, emission minimisation, and at the same time the system transmission loss.
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10.1016/j.ejmg.2021.104264
Arg229Ter) and a whole gene deletion of the HNF1B gene.
Arg229Ter) and a whole gene deletion of the HNF1B gene.
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10.5799/jmid.951502
Methods: Six isolates of Escherichia coli, harboring blaNDM-4 were confirmed by PCR sequencing of the whole gene.
Methods: Six isolates of Escherichia coli, harboring blaNDM-4 were confirmed by PCR sequencing of the whole gene.
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10.1007/s00280-021-04354-7
Whole gene sequencing did not reveal DPYD deleterious allelic variants in the 4 ESRD patients with [U] values > 16 ng/ml.
Whole gene sequencing did not reveal DPYD deleterious allelic variants in the 4 ESRD patients with [U] values > 16 ng/ml.
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10.1016/s0090-8258(21)00736-8
Duplex sequencing, an ultra-accurate error-correction sequencing approach, was used to deeply sequence DNA from lavage samples (average duplex depth ~2500x) with a panel of candidate ovarian cancer driver genes including TP53, ARID1A, PTEN, PPP2R1A, CDKN2A, KRAS (whole genes), CTNNB1, PIK3CA, and BRAF (hotspots only).
Duplex sequencing, an ultra-accurate error-correction sequencing approach, was used to deeply sequence DNA from lavage samples (average duplex depth ~2500x) with a panel of candidate ovarian cancer driver genes including TP53, ARID1A, PTEN, PPP2R1A, CDKN2A, KRAS (whole genes), CTNNB1, PIK3CA, and BRAF (hotspots only).
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10.1007/s13744-021-00895-x
Through continual development and improvement of different methods and sequencing platforms, NGS has promoted mass elucidation of partial or whole genetic materials associated with beneficial insects, pests (of agriculture, forestry and animal, and human health), and species of conservation concern, helping to unravel ecological and evolutionary mechanisms and characterizing survival, trophic interactions, and dispersal.
Through continual development and improvement of different methods and sequencing platforms, NGS has promoted mass elucidation of partial or whole genetic materials associated with beneficial insects, pests (of agriculture, forestry and animal, and human health), and species of conservation concern, helping to unravel ecological and evolutionary mechanisms and characterizing survival, trophic interactions, and dispersal.
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10.1155/2021/4784411
Using the variational expectation-maximization algorithm, the whole generative process model can be inferred.
Using the variational expectation-maximization algorithm, the whole generative process model can be inferred.
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10.7490/F1000RESEARCH.1118484.1
Deciphering this regulatory code, and how the whole gene structure interacts to produce mRNA transcripts and regulate mRNA abundance, can greatly improve our capabilities for controlling gene expression.
Deciphering this regulatory code, and how the whole gene structure interacts to produce mRNA transcripts and regulate mRNA abundance, can greatly improve our capabilities for controlling gene expression.
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10.1210/jendso/bvab104
A whole gene deletion was excluded by microarray, and Sanger sequencing of GC revealed a homozygous pathogenic variant affecting a canonical splice site (c0.
A whole gene deletion was excluded by microarray, and Sanger sequencing of GC revealed a homozygous pathogenic variant affecting a canonical splice site (c0.
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10.1007/s11033-020-06038-6
The mitogenomes of these two species were obtained through whole generation sequencing and annotated.
The mitogenomes of these two species were obtained through whole generation sequencing and annotated.
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10.1371/journal.pgen.1009517
Whole gene deletions of the NF1 gene can cause a more severe phenotype compared to smaller intragenic changes.
Whole gene deletions of the NF1 gene can cause a more severe phenotype compared to smaller intragenic changes.
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10.1371/journal.pgen.1008887
We conducted a genome wide association study (GWAS) using 197 of the Drosophila Genetic Reference Panel (DGRP) lines, and identified a combination of additive and marginal variants, epistatic interactions, whole genes, and enrichment across interaction networks.
We conducted a genome wide association study (GWAS) using 197 of the Drosophila Genetic Reference Panel (DGRP) lines, and identified a combination of additive and marginal variants, epistatic interactions, whole genes, and enrichment across interaction networks.
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10.1111/jep.13534
This study evaluated whether SSU opening differentially modified in-hospital indicators at a whole general hospital and at its cardiology division (CARD).
This study evaluated whether SSU opening differentially modified in-hospital indicators at a whole general hospital and at its cardiology division (CARD).
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10.4236/JBM.2021.92007
Then, the product was purified and sequenced to acquire the whole gene sequence of the N protein and its encoded amino acid sequence.
Then, the product was purified and sequenced to acquire the whole gene sequence of the N protein and its encoded amino acid sequence.
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10.1101/2021.06.23.449585
By examining the biosynthesis of the anti-tubercular wollamides, we show how whole gene duplication and neofunctionalization can result in pathway bifurcation.
By examining the biosynthesis of the anti-tubercular wollamides, we show how whole gene duplication and neofunctionalization can result in pathway bifurcation.
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10.1007/s11159-020-09880-9
The closure of schools, universities and technical institutions around the world has disrupted the lives and learning of a whole generation of students.
The closure of schools, universities and technical institutions around the world has disrupted the lives and learning of a whole generation of students.
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10.1128/AEM.00268-21
cerevisiae D452-2 strain, as well as vigorous expression of whole genes in the DHA-pathway (Candid utilis glycerol facilitator, Ogataea polymorpha glycerol dehydrogenase, endogenous dihydroxyacetone kinase, and triosephosphate isomerase).
cerevisiae D452-2 strain, as well as vigorous expression of whole genes in the DHA-pathway (Candid utilis glycerol facilitator, Ogataea polymorpha glycerol dehydrogenase, endogenous dihydroxyacetone kinase, and triosephosphate isomerase).
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10.1016/j.xplc.2021.100185
The phasing of Iso-Seq data provided a great advantage in separating the whole gene structure and producing a significantly higher separation ratio than RNA-Seq.
The phasing of Iso-Seq data provided a great advantage in separating the whole gene structure and producing a significantly higher separation ratio than RNA-Seq.
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10.1108/S2055-364120200000035005
This text provides comprehensive process and strategies to equip curriculum designers and educators as they guide a whole generation to a bright, safe and beautiful future.
This text provides comprehensive process and strategies to equip curriculum designers and educators as they guide a whole generation to a bright, safe and beautiful future.
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10.3389/fgene.2021.682050
This approach allowed the identification of 26 patients carrying a whole gene CNV of PMP22.
This approach allowed the identification of 26 patients carrying a whole gene CNV of PMP22.
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10.1101/2021.03.16.435537
We show using simulated data that DENR clearly outperforms simple read-count-based methods for estimating the abundances of both whole genes and isoforms.
We show using simulated data that DENR clearly outperforms simple read-count-based methods for estimating the abundances of both whole genes and isoforms.
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Kit Gene
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