sequencing data trang 11 tải miễn phí từ TAILIEUCHUNG

"sequencing data" trang 11 - tải miễn phí từ Tailieuchung

A robust nonlinear low-dimensional manifold for single cell RNA-seq data

A robust nonlinear low-dimensional manifold for single cell RNA-seq data

15 46 1

ScTyper: A comprehensive pipeline for the cell typing analysis of single-cell RNA-seq data

ScTyper: A comprehensive pipeline for the cell typing analysis of single-cell RNA-seq data

8 47 1

RACS: Rapid analysis of ChIP-Seq data for contig based genomes

RACS: Rapid analysis of ChIP-Seq data for contig based genomes

17 54 1

Illumina error correction near highly repetitive DNA regions improves de novo genome assembly

Illumina error correction near highly repetitive DNA regions improves de novo genome assembly

13 60 1

Polymorphic edge detection (PED): Two efficient methods of polymorphism detection from next-generation sequencing data

Polymorphic edge detection (PED): Two efficient methods of polymorphism detection from next-generation sequencing data

12 57 1

RESCUE: Imputing dropout events in singlecell RNA-sequencing data

RESCUE: Imputing dropout events in singlecell RNA-sequencing data

11 24 1

An integrated package for bisulfite DNA methylation data analysis with Indelsensitive mapping

An integrated package for bisulfite DNA methylation data analysis with Indelsensitive mapping

11 46 1

Isma: An R package for the integrative analysis of mutations detected by multiple pipelines

Isma: An R package for the integrative analysis of mutations detected by multiple pipelines

9 72 1

VarGenius executes cohort-level DNA-seq variant calling and annotation and allows to manage the resulting data through a PostgreSQL database

VarGenius executes cohort-level DNA-seq variant calling and annotation and allows to manage the resulting data through a PostgreSQL database

14 34 1

Gene length corrected trimmed mean of M-values (GeTMM) processing of RNA-seq data performs similarly in intersample analyses while improving intrasample comparisons

Gene length corrected trimmed mean of M-values (GeTMM) processing of RNA-seq data performs similarly in intersample analyses while improving intrasample comparisons

13 45 1

Benchmarking differential expression analysis tools for RNA-Seq: Normalization-based vs. log-ratio transformation-based methods

Benchmarking differential expression analysis tools for RNA-Seq: Normalization-based vs. log-ratio transformation-based methods

15 34 1

Matataki: An ultrafast mRNA quantification method for large-scale reanalysis of RNASeq data

Matataki: An ultrafast mRNA quantification method for large-scale reanalysis of RNASeq data

9 44 1

XenofilteR: Computational deconvolution of mouse and human reads in tumor xenograft sequence data

XenofilteR: Computational deconvolution of mouse and human reads in tumor xenograft sequence data

15 34 1

A randomized approach to speed up the analysis of large-scale read-count data in the application of CNV detection

A randomized approach to speed up the analysis of large-scale read-count data in the application of CNV detection

11 39 1

Alignment-free clustering of large data sets of unannotated protein conserved regions using minhashing

Alignment-free clustering of large data sets of unannotated protein conserved regions using minhashing

18 57 1

An information-theoretic approach to the modeling and analysis of whole-genome bisulfite sequencing data

An information-theoretic approach to the modeling and analysis of whole-genome bisulfite sequencing data

23 64 1

Ioncopy: An R Shiny app to call copy number alterations in targeted NGS data

Ioncopy: An R Shiny app to call copy number alterations in targeted NGS data

4 46 1

A sensitive short read homology search tool for paired-end read sequencing data

A sensitive short read homology search tool for paired-end read sequencing data

13 42 1

Mutation status coupled with RNAsequencing data can efficiently identify important non-significantly mutated genes serving as diagnostic biomarkers of endometrial cancer

Mutation status coupled with RNAsequencing data can efficiently identify important non-significantly mutated genes serving as diagnostic biomarkers of endometrial cancer

11 63 1

Using 16S rRNA gene as marker to detect unknown bacteria in microbial communities

Using 16S rRNA gene as marker to detect unknown bacteria in microbial communities

7 53 1

Đầu
1
2
3
4
5
6
7
8
9
10
[ 11 ]
12
13
14
15
Cuối

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.