"DNA sequencing data" trang 1 - tải miễn phí từ tailieunhanh
SCSIM: Jointly simulating correlated single-cell and bulk next-generation DNA sequencing data

SCSIM: Jointly simulating correlated single-cell and bulk next-generation DNA sequencing data
10    72    1
A comparison of three variant calling pipelines using simulated data

A comparison of three variant calling pipelines using simulated data
7    3    1
Calculation of Tajima’s D and other neutrality test statistics from low depth next-generation sequencing data

Calculation of Tajima’s D and other neutrality test statistics from low depth next-generation sequencing data
14    45    1
Characterization of background noise in capture-based targeted sequencing data

Characterization of background noise in capture-based targeted sequencing data
13    51    1
DiNAMO: Highly sensitive DNA motif discovery in high-throughput sequencing data

DiNAMO: Highly sensitive DNA motif discovery in high-throughput sequencing data
10    70    1
Norgal: Extraction and de novo assembly of mitochondrial DNA from whole-genome sequencing data

Norgal: Extraction and de novo assembly of mitochondrial DNA from whole-genome sequencing data
7    79    1
Estimation of the methylation pattern distribution from deep sequencing data

Estimation of the methylation pattern distribution from deep sequencing data
11    64    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    54    1
Characterizing the properties of bisulfite sequencing data: Maximizing power and sensitivity to identify between-group differences in DNA methylation

Characterizing the properties of bisulfite sequencing data: Maximizing power and sensitivity to identify between-group differences in DNA methylation
16    37    1
Methods for copy number aberration detection from single-cell DNA-sequencing data

Methods for copy number aberration detection from single-cell DNA-sequencing data
22    46    1
A study on fast calling variants from nextgeneration sequencing data using decision tree

A study on fast calling variants from nextgeneration sequencing data using decision tree
14    63    1
Probabilistic alignment leads to improved accuracy and read coverage for bisulfite sequencing data

Probabilistic alignment leads to improved accuracy and read coverage for bisulfite sequencing data
8    39    1
NanoMod: A computational tool to detect DNA modifications using Nanopore longread sequencing data

NanoMod: A computational tool to detect DNA modifications using Nanopore longread sequencing data
12    35    1
SLIM: A flexible web application for the reproducible processing of environmental DNA metabarcoding data

SLIM: A flexible web application for the reproducible processing of environmental DNA metabarcoding data
6    53    1
HPG pore: An efficient and scalable framework for nanopore sequencing data

HPG pore: An efficient and scalable framework for nanopore sequencing data
7    35    1
The MOBSTER R package for tumour subclonal deconvolution from bulk DNA whole‑genome sequencing data

The MOBSTER R package for tumour subclonal deconvolution from bulk DNA whole‑genome sequencing data
11    45    1
ANGSD: Analysis of next generation sequencing data

ANGSD: Analysis of next generation sequencing data
13    61    1
Enhancing the detection of barcoded reads in high throughput DNA sequencing data by controlling the false discovery rate

Enhancing the detection of barcoded reads in high throughput DNA sequencing data by controlling the false discovery rate
16    49    1
ReSeq simulates realistic Illumina high-throughput sequencing data

ReSeq simulates realistic Illumina high-throughput sequencing data
37    58    1
DRUMS: Disk Repository with Update Management and Select option for high throughput sequencing data

DRUMS: Disk Repository with Update Management and Select option for high throughput sequencing data
9    67    1