X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (139) 139
humans (103) 103
snv (71) 71
mutation (66) 66
genetics & heredity (53) 53
genomics (51) 51
genomes (49) 49
polymorphism, single nucleotide (49) 49
analysis (37) 37
female (37) 37
genetic variation (36) 36
genetics (36) 36
algorithms (33) 33
cancer (33) 33
genes (30) 30
genetic aspects (30) 30
male (30) 30
mutations (30) 30
research (30) 30
bioinformatics (28) 28
snvs (28) 28
biotechnology & applied microbiology (27) 27
dna sequencing (26) 26
genome (26) 26
identification (26) 26
genetic predisposition to disease (25) 25
software (25) 25
variants (23) 23
mathematical & computational biology (22) 22
nucleotide sequencing (22) 22
gene (21) 21
high-throughput nucleotide sequencing (21) 21
single nucleotide variant (21) 21
biochemistry & molecular biology (20) 20
database (19) 19
disease (19) 19
animals (18) 18
deoxyribonucleic acid--dna (18) 18
next-generation sequencing (18) 18
phenotype (18) 18
adult (17) 17
article (17) 17
biochemical research methods (17) 17
framework (17) 17
nonsynonymous snvs (17) 17
proteins (17) 17
biology (16) 16
high-throughput nucleotide sequencing - methods (16) 16
machine learning (16) 16
risk (16) 16
sequence analysis, dna (16) 16
single nucleotide variants (16) 16
alleles (15) 15
discovery (15) 15
expression (15) 15
single nucleotide polymorphisms (15) 15
association (14) 14
computational biology - methods (14) 14
gene mutations (14) 14
genetic research (14) 14
genotype (14) 14
middle aged (14) 14
snp (14) 14
medicine (13) 13
research article (13) 13
computational biology (12) 12
genome, human (12) 12
genome-wide association study (12) 12
molecular biology (12) 12
ngs (12) 12
pathogenicity (12) 12
polymorphism, single nucleotide - genetics (12) 12
whole genome sequencing (12) 12
cell biology (11) 11
databases, genetic (11) 11
exome sequencing (11) 11
gene expression (11) 11
gene frequency (11) 11
neoplasms - genetics (11) 11
usage (11) 11
variant calling (11) 11
whole exome sequencing (11) 11
aged (10) 10
classification (10) 10
dna (10) 10
gene sequencing (10) 10
nucleotides (10) 10
oncology (10) 10
pedigree (10) 10
phenotypes (10) 10
prediction (10) 10
snv, single nucleotide variant (10) 10
structural variation (10) 10
amino acids (9) 9
amino-acid substitutions (9) 9
biochemistry (9) 9
datasets (9) 9
indel (9) 9
phylogeny (9) 9
research paper (9) 9
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Computational and Structural Biotechnology Journal, ISSN 2001-0370, 2018, Volume 16, pp. 15 - 24
Detection of somatic mutations holds great potential in cancer treatment and has been a very active research field in the past few years, especially since the... 
Somatic mutation | Benchmarking | Unique molecular identifier | Low-frequency mutation | Variant calling | AMPLICON | MUTATION DETECTION | BIOCHEMISTRY & MOLECULAR BIOLOGY | ACCURATE DETECTION | IDENTIFICATION | CANCER | DISCOVERY | POINT MUTATIONS | DNA | FRAMEWORK | SNV DETECTION
Journal Article
by Guo, Y and Yu, H and Samuels, DC and Yue, W and Ness, S and Zhao, YY
BRIEFINGS IN FUNCTIONAL GENOMICS, ISSN 2041-2649, 01/2019, Volume 18, Issue 1, pp. 30 - 39
Through analysis of paired high-throughput DNA-Seq and RNA-Seq data, researchers quickly recognized that RNA-Seq can be used for more than just gene expression... 
RNA editing | WIDE IDENTIFICATION | ADAR | ACCURATE IDENTIFICATION | non-canonical RNA editing | GENOME | SNP | MESSENGER-RNA | DATABASE | RNA-Seq | PARALLEL DNA | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | SITES | FRAMEWORK | SNV | DIVERSITY | MUTATIONS | Sequence Analysis, RNA - methods | RNA Editing | Humans | Transcriptome | Polymorphism, Single Nucleotide | Genome, Human | Genomics - methods | RNA - genetics
Journal Article
Current Protocols in Bioinformatics, ISSN 1934-3396, 2016, Volume 2016, pp. 15.10.1 - 15.10.18
CaVEMan is an expectation maximization-based somatic substitution-detection algorithm that is written in C. The algorithm analyzes sequence data from a test... 
Somatic | SNV | Substitution | Sequencing | Cancer | Computational Biology - methods | Algorithms | Neoplasms - genetics | Humans | Polymorphism, Single Nucleotide - genetics | Genetic Variation - genetics | Software | Genome
Journal Article
BMC Bioinformatics, ISSN 1471-2105, 01/2017, Volume 18, Issue 1
Journal Article
Chemometrics and Intelligent Laboratory Systems, ISSN 0169-7439, 08/2016, Volume 156, pp. 224 - 230
Journal Article