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genome
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DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
science
machine-learning
bioinformatics
deep-learning
genomics
genome
tensorflow
ngs
sequencing
dna
deep-neural-network
deepvariant
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Sep 17, 2021 - Python
Using artificial intelligence and genetic algorithms to automatically write programs. Tutorial: http://www.primaryobjects.com/cms/article149
c-sharp
programming-language
ai
genome
genetic-algorithm
program-synthesis
artificial-intelligence
genetic-programming
genetic-algorithms
fitness-score
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Oct 7, 2020 - C#
fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing
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Jul 19, 2021 - Nim
Personalized Genomics and Proteomics. Main diet: Ensembl, side dishes: SNPs
bioinformatics
snps
medicine
genomics
genome
cancer
biology
vcf
ensembl
medical
cancer-genomics
genome-annotation
proteomics
gtf
bed
cancer-genomes
genome-sequencing
genome-browser
genomes
csv-parser
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Sep 16, 2021 - Python
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Sep 10, 2021 - C++
karyoploteR - An R/Bioconductor package to plot arbitrary data along the genome
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Aug 30, 2021 - R
GenomeTools genome analysis system.
ruby
python
c
library
bioinformatics
lua
annotation
genomics
genome
gff3
repeats
genometools
toolkit
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Sep 15, 2021 - C
A genome browser that shows long reads and complex variants better
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Aug 14, 2021 - JavaScript
Next generation sequencing reads de novo assembler.
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Apr 19, 2021 - C
Viral genomics analysis pipelines
genomics
genome
variant-calling
bam
genome-sequencing
illumina
fastq
genome-assembly
variant-annotations
viral-ngs
viral
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Nov 3, 2020 - Python
Genomic Data Retrieval with R
r
genomics
genome
metagenomics
rstats
genome-annotation
r-package
meta-analysis
genome-retrieval
biomart
database-retrieval
ncbi-genbank
ensembl-servers
sequenced-genomes
proteome
peer-reviewed
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Mar 18, 2021 - R
Genome annotation with AUGUSTUS
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Sep 13, 2021 - C++
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Sep 1, 2021 - M4
DNABERT: pre-trained Bidirectional Encoder Representations from Transformers model for DNA-language in genome
nlp
machine-learning
natural-language-processing
deep-learning
genome
gpu
sequence
kmer
dnabert-model
kmer-format
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Aug 27, 2021 - Python
Nanopore sequence read simulator
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Sep 17, 2021 - Python
machine learning for genomic variants
emr
aws
bioinformatics
gwas
genome
random-forest
notebook
vcf
databricks
association-studies
variant-spark
variantspark
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Sep 6, 2021 - JavaScript
Raw dump of Kenneth Reitz's DNA Sequence, Ancestry, Genealogy, &c.
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Oct 2, 2019 - HTML
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Sep 9, 2021 - C++
Dotplot large Genomes in an Interactive, Efficient and Simple way
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Apr 7, 2021 - Python
A package for designing compact and comprehensive capture probe sets.
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Jan 26, 2021 - Python
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In some metagenomic contexts, there can be closely related species in a sample that can make read mapping to a single reference genome difficult (e.g. cross-mapping of reads between species). In this situation, it can be useful to employ competitive mapping, whereby reference genomes from closely related species are concatenated (in a multifasta), and the reads mapped to this reference. This can a