"NGS data" trang 1 - tải miễn phí từ tailieunhanh
NGS-Integrator: An efficient tool for combining multiple NGS data tracks using minimum Bayes’ factors

NGS-Integrator: An efficient tool for combining multiple NGS data tracks using minimum Bayes’ factors
7    52    1
SeqPurge: Highly-sensitive adapter trimming for paired-end NGS data

SeqPurge: Highly-sensitive adapter trimming for paired-end NGS data
7    45    1
TRAPLINE: A standardized and automated pipeline for RNA sequencing data analysis, evaluation and annotation

TRAPLINE: A standardized and automated pipeline for RNA sequencing data analysis, evaluation and annotation
11    74    1
Non-synonymous variations in cancer and their effects on the human proteome: Workflow for NGS data biocuration and proteome-wide analysis of TCGA data

Non-synonymous variations in cancer and their effects on the human proteome: Workflow for NGS data biocuration and proteome-wide analysis of TCGA data
18    46    1
SUSHI: An exquisite recipe for fully documented, reproducible and reusable NGS data analysis

SUSHI: An exquisite recipe for fully documented, reproducible and reusable NGS data analysis
9    47    1
4Pipe4 – A 454 data analysis pipeline for SNP detection in datasets with no reference sequence or strain information

4Pipe4 – A 454 data analysis pipeline for SNP detection in datasets with no reference sequence or strain information
6    35    1
Sketch distance-based clustering of chromosomes for large genome database compression

Sketch distance-based clustering of chromosomes for large genome database compression
9    27    2
NexGenEx-Tom: A gene expression platform to investigate the functionalities of the tomato genome

NexGenEx-Tom: A gene expression platform to investigate the functionalities of the tomato genome
13    131    0
An approach to forecast human cancer by profiling microRNA expressions from NGS data

An approach to forecast human cancer by profiling microRNA expressions from NGS data
9    33    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    43    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    73    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    65    1
PSE-HMM: Genome-wide CNV detection from NGS data using an HMM with Position-Specific Emission probabilities

PSE-HMM: Genome-wide CNV detection from NGS data using an HMM with Position-Specific Emission probabilities
11    36    1
Cnidaria: Fast, reference-free clustering of raw and assembled genome and transcriptome NGS data

Cnidaria: Fast, reference-free clustering of raw and assembled genome and transcriptome NGS data
10    57    1
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    37    1
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    55    1
ImmunExplorer (IMEX): A software framework for diversity and clonality analyses of immunoglobulins and T cell receptors on the basis of IMGT/HighV-QUEST preprocessed NGS data

ImmunExplorer (IMEX): A software framework for diversity and clonality analyses of immunoglobulins and T cell receptors on the basis of IMGT/HighV-QUEST preprocessed NGS data
10    41    1
UrQt: An efficient software for the Unsupervised Quality trimming of NGS data

UrQt: An efficient software for the Unsupervised Quality trimming of NGS data
8    46    1
Launching genomics into the cloud: Deployment of Mercury, a next generation sequence analysis pipeline

Launching genomics into the cloud: Deployment of Mercury, a next generation sequence analysis pipeline
11    55    1
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    49    1