sequencing data trang 5 tải miễn phí từ TAILIEUCHUNG

"sequencing data" trang 5 - tải miễn phí từ Tailieuchung

ADEPT, a dynamic next generation sequencing data error-detection program with trimming

ADEPT, a dynamic next generation sequencing data error-detection program with trimming

7 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

CloneCNA: Detecting subclonal somatic copy number alterations in heterogeneous tumor samples from whole-exome sequencing data

CloneCNA: Detecting subclonal somatic copy number alterations in heterogeneous tumor samples from whole-exome sequencing data

10 81 1

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

Optimized pipeline of MuTect and GATK tools to improve the detection of somatic single nucleotide polymorphisms in wholeexome sequencing data

Optimized pipeline of MuTect and GATK tools to improve the detection of somatic single nucleotide polymorphisms in wholeexome sequencing data

9 65 1

Evaluating the necessity of PCR duplicate removal from next-generation sequencing data and a comparison of approaches

Evaluating the necessity of PCR duplicate removal from next-generation sequencing data and a comparison of approaches

10 46 1

ContextMap 2: Fast and accurate context-based RNA-seq mapping

ContextMap 2: Fast and accurate context-based RNA-seq mapping

15 31 1

Estimation of the methylation pattern distribution from deep sequencing data

Estimation of the methylation pattern distribution from deep sequencing data

11 43 1

AllelicImbalance: An R/ bioconductor package for detecting, managing, and visualizing allele expression imbalance data from RNA sequencing

AllelicImbalance: An R/ bioconductor package for detecting, managing, and visualizing allele expression imbalance data from RNA sequencing

6 33 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

Odintifier - A computational method for identifying insertions of organellar origin from modern and ancient high-throughput sequencing data based on haplotype phasing

Odintifier - A computational method for identifying insertions of organellar origin from modern and ancient high-throughput sequencing data based on haplotype phasing

13 48 1

WiseScaffolder: An algorithm for the semi-automatic scaffolding of Next Generation Sequencing data

WiseScaffolder: An algorithm for the semi-automatic scaffolding of Next Generation Sequencing data

13 54 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

BSPAT: A fast online tool for DNA methylation co-occurrence pattern analysis based on high-throughput bisulfite sequencing data

BSPAT: A fast online tool for DNA methylation co-occurrence pattern analysis based on high-throughput bisulfite sequencing data

9 37 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

The HTS barcode checker pipeline, a tool for automated detection of illegally traded species from high-throughput sequencing data

The HTS barcode checker pipeline, a tool for automated detection of illegally traded species from high-throughput sequencing data

8 32 1

HECTOR: A parallel multistage homopolymer spectrum based error corrector for 454 sequencing data

HECTOR: A parallel multistage homopolymer spectrum based error corrector for 454 sequencing data

13 42 1

An integrative method to normalize RNA-Seq data

An integrative method to normalize RNA-Seq data

11 23 1

Clinical PathoScope: Rapid alignment and filtration for accurate pathogen identification in clinical samples using unassembled sequencing data

Clinical PathoScope: Rapid alignment and filtration for accurate pathogen identification in clinical samples using unassembled sequencing data

14 32 1

Masking as an effective quality control method for next-generation sequencing data analysis

Masking as an effective quality control method for next-generation sequencing data analysis

8 36 1

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