Topic: whole-exome-sequencing Goto Github
Some thing interesting about whole-exome-sequencing
Some thing interesting about whole-exome-sequencing
whole-exome-sequencing,An adaptable method for analyzing SNVs, INDELs, and CNVs from Whole Exome Sequencing (WES) data, emphasizing germline variants.
User: anbianchi
Home Page: https://github.com/anbianchi/IntegratedSNVINDELSandCNV
whole-exome-sequencing,Scripts and data processing notes for Russian exome sequencing AF paper
Organization: bioinf
whole-exome-sequencing,
Organization: bioinf
whole-exome-sequencing,Analyses and figures related to Mossanen and Carvalho et al Eur Urol 2021 manuscript entitled "Genomic Features of Muscle-Invasive Bladder Cancer Arising After Prostate Radiotherapy"
User: carvalhofilipel
whole-exome-sequencing,An open-source and scalable solution to NGS analysis powered by the NIH's Biowulf cluster.
Organization: ccbr
whole-exome-sequencing,esohinformatics
User: esohkevin
Home Page: https://esohkevin.github.io
whole-exome-sequencing,Genetic Medicine of African Populations
Organization: genemap-research
Home Page: https://genemap-research.github.io/
whole-exome-sequencing,Workflows for whole-genome/exome sequencing data analysis
Organization: genemap-research
Home Page: https://genemap-research.github.io/docs/workflows/ngs/
whole-exome-sequencing,Research projects conducted at the GeneMAP Research Center
Organization: genemap-research
Home Page: https://genemap-research.github.io/docs/projects/
whole-exome-sequencing,SeqMeta pipeline
Organization: genepi-freiburg
whole-exome-sequencing,WDL-based pipelines
Organization: genomicsiter-developers
whole-exome-sequencing,Whole Exome/Whole Genome Sequencing alignment pipeline
Organization: iarcbioinfo
whole-exome-sequencing,Pipeline for copy number variant calling from Whole Exome sequencing data using CODEX
Organization: iarcbioinfo
whole-exome-sequencing,Bio Big Data and Precision Medicine Training Course
User: jeongu
whole-exome-sequencing,Constructing Neoantigen Vaccine Pipeline with pVACtools
User: jeongu
whole-exome-sequencing,END OF MASTER'S PROJECT: Valencian International University VIU
User: juancarlosbio
whole-exome-sequencing,Workspace for data science projects and NGS pipelines. Contains RStudio, Jupyter Notebook, VSCode and file manager. Can connect to Tailscale network to bypass firewalls.
User: kstawiski
whole-exome-sequencing,An automated tool for processing whole-exome sequencing data
Organization: labbcb
Home Page: https://bcblab.org/hpexome/
whole-exome-sequencing,Analysis documentation for research into the variants associated with hyperparathyroidism. Illumina, germline, human, whole exome sequence (WES) data from the CCDHB.
User: leahkemp
whole-exome-sequencing,📑 A library of example code -aka cheatsheets- for tools I use or analyses I carry out pretty often. This repo doubles as an easy way to find the code I need without going through all my scripts.
User: ledakatopodi
whole-exome-sequencing,An app for automatically functionally annotating the variants of whole-genome/whole-exome sequencing (WGS/WES) studies and integrating the functional annotations with the genotype data using FAVORannotator in UK Biobank RAP
Organization: li-lab-genetics
whole-exome-sequencing,An app for performing association analysis of whole-genome/whole-exome sequencing (WGS/WES) studies using STAARpipeline in UK Biobank RAP
Organization: li-lab-genetics
whole-exome-sequencing,An app for summarizing association analysis results of whole-genome/whole-exome sequencing (WGS/WES) studies in UK Biobank RAP
Organization: li-lab-genetics
whole-exome-sequencing,An app for summarizing association analysis results of whole-genome/whole-exome sequencing (WGS/WES) studies in UK Biobank RAP
Organization: li-lab-genetics
whole-exome-sequencing,LOVD+ -- LOVD for diagnostics: analysis of whole-exome data using LOVD.
Organization: lovdnl
Home Page: http://www.LOVD.nl/plus
whole-exome-sequencing,Nature Medicine paper. A Multidimensional Precision Medicine Approach for Autism Subtype Identification.
User: luoyuanlab
whole-exome-sequencing,Whole Exome Sequencing end-to-end pipeline. Starting from whole exome fastq files: Data QC, Adapter Trimming, Reference Genome Alignment, SAM/BAM Validation, Data Recalibration and Variant Calling.
User: mehdimerbah
whole-exome-sequencing,Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
Organization: nf-core
Home Page: https://nf-co.re/sarek
whole-exome-sequencing,Clinical Whole Genome and Exome Sequencing Pipeline
Organization: openomics
Home Page: https://openomics.github.io/genome-seek/
whole-exome-sequencing,Discover VNTR-associated DELs that are hard to find using Illumina reads
User: petermchale
whole-exome-sequencing,STAR-NN: A deep neural network model to predict the risk of ASD using whole exome sequencing dataset
User: qingwu17
whole-exome-sequencing,Automating WES Data analysis (primarily of Cancer).
User: ranjanjs34
whole-exome-sequencing,Code and variants to generate results published in Waller RG et al, Hum Mol Genet, 2021.
User: rosaliegwaller
whole-exome-sequencing,Analysis of paired tumor-normal whole exome sequencing data generated in a pilot open-access study of participants in Texas.
User: sbresnahan
Home Page: http://seantbresnahan.com/TexasCancerGenomics/
whole-exome-sequencing,Code and resources for bioinformatics analyses I've done.
User: sclayton33
whole-exome-sequencing,
User: snewhouse
whole-exome-sequencing,Map and post-process your bams for SNP calling
User: tdayris-perso
whole-exome-sequencing,WES pipeline with customizable scoring system based on 10 criteria.
User: variantcaller
whole-exome-sequencing,
User: vicellken
whole-exome-sequencing,
User: xiaoqiluo
whole-exome-sequencing,An R package for performing association analysis of whole-genome/whole-exome sequencing (WGS/WES) studies using STAARpipeline
User: xihaoli
whole-exome-sequencing,The tutorial for performing single-/multi-trait association analysis of whole-genome/whole-exome sequencing (WGS/WES) studies using FAVORannotator, STAARpipeline and STAARpipelineSummary
User: xihaoli
whole-exome-sequencing,An R package for summarizing and visualizing association analysis results of whole-genome/whole-exome sequencing (WGS/WES) studies generated by STAARpipeline
User: xihaoli
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