"next generation sequencing" trang 9 - tải miễn phí từ tailieuXANH
ClinQC: A tool for quality control and cleaning of Sanger and NGS data in clinical research

ClinQC: A tool for quality control and cleaning of Sanger and NGS data in clinical research
9    123    0
Empirical estimation of sequencing error rates using smoothing splines

Empirical estimation of sequencing error rates using smoothing splines
11    81    0
Detection and sequence/structure mapping of biophysical constraints to protein variation in saturated mutational libraries and protein sequence alignments with a dedicated server

Detection and sequence/structure mapping of biophysical constraints to protein variation in saturated mutational libraries and protein sequence alignments with a dedicated server
13    63    0
Consistency of biological networks inferred from microarray and sequencing data

Consistency of biological networks inferred from microarray and sequencing data
10    169    0
An Atlas of annotations of Hydra vulgaris transcriptome

An Atlas of annotations of Hydra vulgaris transcriptome
7    62    0
Analysis of amplicon-based NGS data from neurological disease gene panels: A new method for allele drop-out management

Analysis of amplicon-based NGS data from neurological disease gene panels: A new method for allele drop-out management
12    66    0
Evaluation of variant detection software for pooled next-generation sequence data

Evaluation of variant detection software for pooled next-generation sequence data
9    64    0
Error correction and statistical analyses for intra-host comparisons of feline immunodeficiency virus diversity from high-throughput sequencing data

Error correction and statistical analyses for intra-host comparisons of feline immunodeficiency virus diversity from high-throughput sequencing data
14    78    0
Reference-free compression of high throughput sequencing data with a probabilistic de Bruijn graph

Reference-free compression of high throughput sequencing data with a probabilistic de Bruijn graph
14    40    0
ShatterProof: Operational detection and quantification of chromothripsis

ShatterProof: Operational detection and quantification of chromothripsis
13    63    0
Pollux: Platform independent error correction of single and mixed genomes

Pollux: Platform independent error correction of single and mixed genomes
12    54    0
Identification of indels in next-generation sequencing data

Identification of indels in next-generation sequencing data
8    70    0
CIRCUS: A package for Circos display of structural genome variations from paired-end and mate-pair sequencing data

CIRCUS: A package for Circos display of structural genome variations from paired-end and mate-pair sequencing data
6    61    0
Clinical phenotype-based gene prioritization: An initial study using semantic similarity and the human phenotype ontology

Clinical phenotype-based gene prioritization: An initial study using semantic similarity and the human phenotype ontology
11    57    0
MendeLIMS: A web-based laboratory information management system for clinical genome sequencing

MendeLIMS: A web-based laboratory information management system for clinical genome sequencing
8    174    0
A Hidden Markov Model for identifying essential and growth-defect regions in bacterial genomes from transposon insertion sequencing data

A Hidden Markov Model for identifying essential and growth-defect regions in bacterial genomes from transposon insertion sequencing data
12    70    0
Diminishing return for increased Mappability with longer sequencing reads: Implications of the k-mer distributions in the human genome

Diminishing return for increased Mappability with longer sequencing reads: Implications of the k-mer distributions in the human genome
12    55    0
Routine performance and errors of 454 HLA exon sequencing in diagnostics

Routine performance and errors of 454 HLA exon sequencing in diagnostics
8    52    0
MethyQA: A pipeline for bisulfite-treated methylation sequencing quality assessment

MethyQA: A pipeline for bisulfite-treated methylation sequencing quality assessment
9    63    0
Comparing a few SNP calling algorithms using low-coverage sequencing data

Comparing a few SNP calling algorithms using low-coverage sequencing data
15    70    0
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