Python GraphQL Client - PyGQLC
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Updated
May 21, 2024 - Python
Python GraphQL Client - PyGQLC
Regexp based tool for mutating generic source code across numerous languages
🧬 Chromatogram File Utils, a package that integrates trace visualization, mutation calling and quality control for Sanger sequencing data.
Snakemake Pipeline for the Analyses of ChIP-seq data in Cancer samples
The Cancer Genome Atlas (TCGA), a cancer genomics reference program, has molecularly characterized more than 20,000 primary cancer samples and paired normal samples covering 33 types of cancer. This joint effort between the NCI and the National Human Genome Research Institute began in 2006.
Official repository for the paper "Few-shot Prediction of the experimental functional measurements for proteins with single point mutations".
During the progression of cancer cells, the degree of genome instability increases leading to genome chaos in populations of malignant cells. While normally chaos is associated with ergodicity, i.e., the state when the time average of relevant parameters is equal to the phase space average, the situation with cancer propagation is more complex.
A bioinformatics pipeline to identify the best available PDB structures for all available variants for specified genes of interest
Generating random mutations
Customizable permissions for graphene-django.
A tool for fast and accurate summarizing of variant calling format (VCF) files
Chromosomal mutations associated with nitrofurantoin resistance in Escherichia coli
MSc Bioinformatics with Systems Biology Dissertation
SARS-Cov-2 Recombinant Finder for fasta sequences
Automated analysis tool for mutations in promoters, transcription factor binding sites, coding regions and protein domains in the context of gene regulatory networks.
Predicting the effect of mutations on protein stability and protein-protein interaction affinity.
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