vSNP -- validate SNPs
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Updated
Jun 25, 2024 - Python
vSNP -- validate SNPs
Generate an interactive HTML-based report from M.tb SnpEff annotated VCF(s)
Visualize microbial evolution at the SNP level!
to analyze multiple VCF files and generate a summary of variant metrics
API to read, write, and filter DNA sequence alignment files
Lightweight standalone tool to reduce size of VCF files through filtering
create a interactive coverage plot dashboard from bam files and add gb, vcf and bed tracks
It reads all values in certain rows and columns in Excel and converts phone number values to vcf. It can be converted to vcf by typing the prefix we want to add to the required section in the code. Adds phone numbers to our contact list in seconds. It has a simple and useful interface.
CNV analysis based on the depth of coverage of Illumina data
A python library to develop genomic data simulators
Convert SNPs in VCF format to PHYLIP, NEXUS, binary NEXUS, or FASTA alignments for phylogenetic analysis
A simple Python script for extracting images out of an "SMS Backup & Restore" backup.
A quick way to visualize VCF data in a html report
Bioinformatics
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