"Whole genome sequencing data" trang 1 - tải miễn phí từ tailieunhanh
ALPHLARD: A Bayesian method for analyzing HLA genes from whole genome sequence data

ALPHLARD: A Bayesian method for analyzing HLA genes from whole genome sequence data
11    44    1
Quantifying the mapping precision of genome-wide association studies using whole-genome sequencing data

Quantifying the mapping precision of genome-wide association studies using whole-genome sequencing data
10    95    3
Seq-seq-pan: Building a computational pan-genome data structure on whole genome alignment

Seq-seq-pan: Building a computational pan-genome data structure on whole genome alignment
12    53    1
Identifying and mitigating batch effects in whole genome sequencing data

Identifying and mitigating batch effects in whole genome sequencing data
12    58    1
Gen2Epi: An automated whole-genome sequencing pipeline for linking full genomes to antimicrobial susceptibility and molecular epidemiological data in Neisseria gonorrhoeae

Gen2Epi: An automated whole-genome sequencing pipeline for linking full genomes to antimicrobial susceptibility and molecular epidemiological data in Neisseria gonorrhoeae
11    47    1
Assessing genomic diversity and signatures of selection in Original Braunvieh cattle using whole-genome sequencing data

Assessing genomic diversity and signatures of selection in Original Braunvieh cattle using whole-genome sequencing data
14    14    2
ExpansionHunter Denovo: A computational method for locating known and novel repeat expansions in short-read sequencing data

ExpansionHunter Denovo: A computational method for locating known and novel repeat expansions in short-read sequencing data
14    14    1
Wg-blimp: An end-to-end analysis pipeline for whole genome bisulfite sequencing data

Wg-blimp: An end-to-end analysis pipeline for whole genome bisulfite sequencing data
8    49    1
STRScan: Targeted profiling of short tandem repeats in whole-genome sequencing data

STRScan: Targeted profiling of short tandem repeats in whole-genome sequencing data
6    42    1
PennCNV in whole-genome sequencing data

PennCNV in whole-genome sequencing data
8    66    1
Evaluation of tools for identifying large copy number variations from ultra-lowcoverage whole-genome sequencing data

Evaluation of tools for identifying large copy number variations from ultra-lowcoverage whole-genome sequencing data
15    33    1
MethylStar: A fast and robust pre-processing pipeline for bulk or single-cell whole-genome bisulfite sequencing data

MethylStar: A fast and robust pre-processing pipeline for bulk or single-cell whole-genome bisulfite sequencing data
8    38    2
Performance assessment of variant calling pipelines using human whole exome sequencing and simulated data

Performance assessment of variant calling pipelines using human whole exome sequencing and simulated data
11    64    1
Within-species contamination of bacterial whole-genome sequence data has a greater influence on clustering analyses than between-species contamination

Within-species contamination of bacterial whole-genome sequence data has a greater influence on clustering analyses than between-species contamination
6    47    3
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
QuantTB – a method to classify mixed Mycobacterium tuberculosis infections within whole genome sequencing data

QuantTB – a method to classify mixed Mycobacterium tuberculosis infections within whole genome sequencing data
16    47    2
Genome-wide association mapping of Sclerotinia sclerotiorum resistance in soybean using whole-genome resequencing data

Genome-wide association mapping of Sclerotinia sclerotiorum resistance in soybean using whole-genome resequencing data
9    48    1
Genomic analyses of the Chlamydia trachomatis core genome show an association between chromosomal genome, plasmid type and disease

Genomic analyses of the Chlamydia trachomatis core genome show an association between chromosomal genome, plasmid type and disease
13    65    1
HGT-ID: An efficient and sensitive workflow to detect human-viral insertion sites using next-generation sequencing data

HGT-ID: An efficient and sensitive workflow to detect human-viral insertion sites using next-generation sequencing data
11    75    1
Extensive genome analysis of Coxiella burnetii reveals limited evolution within genomic groups

Extensive genome analysis of Coxiella burnetii reveals limited evolution within genomic groups
17    35    1