next generation sequencing trang 9 tải miễn phí từ TAILIEUCHUNG

"next generation sequencing" trang 9 - tải miễn phí từ Tailieuchung

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 40 1

Consistency of biological networks inferred from microarray and sequencing data

Consistency of biological networks inferred from microarray and sequencing data

10 17 1

An Atlas of annotations of Hydra vulgaris transcriptome

An Atlas of annotations of Hydra vulgaris transcriptome

7 43 2

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 42 1

Evaluation of variant detection software for pooled next-generation sequence data

Evaluation of variant detection software for pooled next-generation sequence data

9 21 1

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 49 1

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 28 1

ShatterProof: Operational detection and quantification of chromothripsis

ShatterProof: Operational detection and quantification of chromothripsis

13 31 1

Pollux: Platform independent error correction of single and mixed genomes

Pollux: Platform independent error correction of single and mixed genomes

12 24 1

Identification of indels in next-generation sequencing data

Identification of indels in next-generation sequencing data

8 29 1

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 29 1

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 56 1

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 27 1

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 33 1

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 41 1

Routine performance and errors of 454 HLA exon sequencing in diagnostics

Routine performance and errors of 454 HLA exon sequencing in diagnostics

8 12 1

MethyQA: A pipeline for bisulfite-treated methylation sequencing quality assessment

MethyQA: A pipeline for bisulfite-treated methylation sequencing quality assessment

9 6 1

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

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

15 19 1

Comprehensive molecular profiling of Taiwanese breast cancers revealed potential therapeutic targets: Prevalence of actionable mutations among 380 targeted sequencing analyses

Comprehensive molecular profiling of Taiwanese breast cancers revealed potential therapeutic targets: Prevalence of actionable mutations among 380 targeted sequencing analyses

14 39 1

Cruxome: A powerful tool for annotating, interpreting and reporting genetic variants

Cruxome: A powerful tool for annotating, interpreting and reporting genetic variants

9 37 1

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