Pinned Repositories
annot_gnomad
Annotate structural variants in gnomAD
annot_utils
scripts processing annotation data from UCSC
annovar2vcf
under development
Genomon-ITDetector
for detecting internal tandem duplication from genome sequence data.
GenomonBreakPoint
empirical bayesian framework for detecting somatic breakpoints from sequencing data
module_box_kchiba
RefGeneTxtToBed
Convert UCSC refGene.txt to bed format
RNAseq_for_HGC
SvABAvsGenomonSV
The comparison of SvABA and GenomonSV
three-arrowed-vcf-validator
Python tools for validating vcf file
ken0-1n's Repositories
ken0-1n/vcf-validator
Validation suite for Variant Call Format (VCF) files, implemented using C++11
ken0-1n/fusionfusion
script for detecting fusion genes from several transcript alignment tools
ken0-1n/SaltStackTest
SaltStackをAWSで使ってみる
ken0-1n/GenomonBreakPoint
empirical bayesian framework for detecting somatic breakpoints from sequencing data
ken0-1n/genomon_pipeline_cloud
Software for executing genomon pipeline in cloud environments
ken0-1n/AzureBatchTutorialBwa
I am studying Azure Batch using this linked script now.
ken0-1n/paplot
paplot creates various dynamic and interactive reports for cancer genome analysis.
ken0-1n/VCFtoAnnoFormat
ken0-1n/CGC_Docker_Test
ken0-1n/GenomonHotspotBlackList
make cancer hotspot black lists
ken0-1n/GenomonHotspotDatabase
To add the chromosome position in the hotspots.txt
ken0-1n/annovar2vcf
under development
ken0-1n/rna-inframe-checker
Checks, if gene fusion is inframe.
ken0-1n/GenomonPipeline-AWS
ken0-1n/fusion_utils
utility for comparing fusion results
ken0-1n/annot_utils
scripts processing annotation data from UCSC
ken0-1n/GenomonComplexMutation
Detecting complex mutations
ken0-1n/GenomonPipeline-Azure
Using GenomonPipeline version 2.3
ken0-1n/STAR
RNA-seq aligner
ken0-1n/readthedocs.org
source code to readthedocs.org
ken0-1n/pysam
Pysam is a python module for reading and manipulating Samfiles. It's a lightweight wrapper of the samtools C-API. Pysam also includes an interface for tabix.
ken0-1n/GenomonSummary
script for calculating summary
ken0-1n/RealignmentFilter
ken0-1n/s-Pindel-ITD-Detector
a framework for the detection of somatic ITDs using Pindel
ken0-1n/RNAseq_for_HGC
ken0-1n/exome_for_HGC
ken0-1n/clipcrop
a tool for detecting structural variations using soft-clipping information