Efficient genotyping bi-allelic SNPs on single cells
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Updated
Apr 13, 2024 - C
Efficient genotyping bi-allelic SNPs on single cells
Pileup biallelic SNPs from single-cell and bulk RNA-seq data
using all the bits for echt rapid variant annotation and filtering
Regulatory Element Locus Intersection (RELI) Analysis
An R package for the Latent Environmental & Genetic InTeraction (LEGIT) model
Convolutional Embedded Networks for Population Scale Clustering and Bio-ancestry Inferencing
Thesaurus for genetic variants
The general impact of haploinsufficiency on brain connectivity underlies the pleiotropic effect of neuropsychiatric CNVs
The transplot package can be used to make multi-track plots of Next Generation Sequencing (NGS) data for gene transcripts, namely for depth of coverage and for the distribution of variants and protein domains.
Collection of scripts to map eQTL with RNAseq Data and Genotype by Sequencing
Final Project - Post Genomic Analysis
An R package for interpreting genetic variants according to the ACMG guidelines.
Advanced bioinformatics analysis of RNA sequencing data and genomic databases using R. Explore allelic imbalances, SNP variants, and phylogenetic trees to uncover genetic insights and visualize complex data interactions.
Bioinformatic approach to identify functional transcription factor binding motifs
At The ODIN, we believe the future is going to be dominated by genetic engineering and consumer genetic design will be a big part of that. We are making that happen by creating kits and tools that allow anyone to make unique and usable organisms at home or in a lab or anywhere.
DNAc is a programming language for DNAs.
NCBI Medical Genetics, UMLS Unified Medical Language System Concepts and PubMed linked citations
Extracting gene variants from supplemental data files of human genomics research articles.
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