"dna sequencing data" trang 2 - tải miễn phí từ tailieuXANH
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    71    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
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
Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data

Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
18    66    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    388    1
A distance-type measure approach to the analysis of copy number variation in DNA sequencing data

A distance-type measure approach to the analysis of copy number variation in DNA sequencing data
13    133    1
Mitochondrial heteroplasmy in vertebrates using ChIP-sequencing data

Mitochondrial heteroplasmy in vertebrates using ChIP-sequencing data
14    145    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    59    0
Detection and quantification of mitochondrial DNA deletions from nextgeneration sequence data

Detection and quantification of mitochondrial DNA deletions from nextgeneration sequence data
8    53    0
Indel detection from DNA and RNA sequencing data with transIndel

Indel detection from DNA and RNA sequencing data with transIndel
11    355    1
WHAM!: A web-based visualization suite for user-defined analysis of metagenomic shotgun sequencing data

WHAM!: A web-based visualization suite for user-defined analysis of metagenomic shotgun sequencing data
11    157    1
Validation of computational determination of microsatellite status using whole exome sequencing data from colorectal cancer patients

Validation of computational determination of microsatellite status using whole exome sequencing data from colorectal cancer patients
8    59    0
Effects of sample age on data quality from targeted sequencing of museum specimens: What are we capturing in time?

Effects of sample age on data quality from targeted sequencing of museum specimens: What are we capturing in time?
10    120    1
Analysis of the canid Y-chromosome phylogeny using short-read sequencing data reveals the presence of distinct haplogroups among Neolithic European dogs

Analysis of the canid Y-chromosome phylogeny using short-read sequencing data reveals the presence of distinct haplogroups among Neolithic European dogs
9    209    1
Clonealign: Statistical integration of independent single-cell RNA and DNA sequencing data from human cancers

Clonealign: Statistical integration of independent single-cell RNA and DNA sequencing data from human cancers
12    38    1
Performance evaluation of lossy quality compression algorithms for RNA-seq data

Performance evaluation of lossy quality compression algorithms for RNA-seq data
15    44    0
Family reunion via error correction: An efficient analysis of duplex sequencing data

Family reunion via error correction: An efficient analysis of duplex sequencing data
10    53    0
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    185    0
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    66    0
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