"ngs platforms" trang 2 - tải miễn phí từ tailieuXANH
SEQprocess: A modularized and customizable pipeline framework for NGS processing in R package

SEQprocess: A modularized and customizable pipeline framework for NGS processing in R package
7    75    0
GMASS: A novel measure for genome assembly structural similarity

GMASS: A novel measure for genome assembly structural similarity
9    46    0
Web-based design and analysis tools for CRISPR base editing

Web-based design and analysis tools for CRISPR base editing
7    49    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
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    53    0
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    68    0
Je, a versatile suite to handle multiplexed NGS libraries with unique molecular identifiers

Je, a versatile suite to handle multiplexed NGS libraries with unique molecular identifiers
6    60    0
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    62    0
MetaMIS: A metagenomic microbial interaction simulator based on microbial community profiles

MetaMIS: A metagenomic microbial interaction simulator based on microbial community profiles
12    66    0
GenomeCAT: A versatile tool for the analysis and integrative visualization of DNA copy number variants

GenomeCAT: A versatile tool for the analysis and integrative visualization of DNA copy number variants
8    62    0
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    55    0
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    123    0
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    73    0
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    66    0
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    64    0
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    64    0
InteMAP: Integrated metagenomic assembly pipeline for NGS short reads

InteMAP: Integrated metagenomic assembly pipeline for NGS short reads
14    43    0
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    65    0
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    55    0
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    59    0
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