"sequencing data" trang 5 - 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
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    80    0
Consistency of biological networks inferred from microarray and sequencing data

Consistency of biological networks inferred from microarray and sequencing data
10    169    0
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    52    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
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    82    0
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    56    0
ContextMap 2: Fast and accurate context-based RNA-seq mapping

ContextMap 2: Fast and accurate context-based RNA-seq mapping
15    70    0
Estimation of the methylation pattern distribution from deep sequencing data

Estimation of the methylation pattern distribution from deep sequencing data
11    69    0
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    49    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
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    45    0
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    44    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
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    70    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
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    74    0
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    87    0
An integrative method to normalize RNA-Seq data

An integrative method to normalize RNA-Seq data
11    62    0
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    101    0
Đã phát hiện trình chặn quảng cáo AdBlock
Trang web này phụ thuộc vào doanh thu từ số lần hiển thị quảng cáo để tồn tại. Vui lòng tắt trình chặn quảng cáo của bạn hoặc tạm dừng tính năng chặn quảng cáo cho trang web này.