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Feb 7, 2018 - JavaScript
#
genome
Here are 276 public repositories matching this topic...
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 10, 2020 - 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 1, 2018 - C#
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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Jul 11, 2020 - Python
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Sep 9, 2020 - C++
karyoploteR - An R/Bioconductor package to plot arbitrary data along the genome
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Sep 9, 2020 - R
GenomeTools genome analysis system.
ruby
python
c
library
bioinformatics
lua
annotation
genomics
genome
gff3
repeats
genometools
toolkit
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Sep 10, 2020 - C
A genome browser that shows long reads and complex variants better
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Aug 14, 2020 - JavaScript
Next generation sequencing reads de novo assembler.
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Jul 23, 2019 - 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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May 20, 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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Aug 8, 2020 - R
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Jul 20, 2020 - M4
Genome annotation with AUGUSTUS
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Sep 11, 2020 - C++
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 10, 2020 - JavaScript
Nanopore sequence read simulator
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Aug 9, 2020 - Python
Raw dump of Kenneth Reitz's DNA Sequence, Ancestry, Genealogy, &c.
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Oct 2, 2019 - HTML
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Aug 30, 2020 - C++
Dotplot large Genomes in an Interactive, Efficient and Simple way
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Sep 3, 2020 - Python
A package for designing compact and comprehensive capture probe sets.
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Jun 12, 2020 - Python
Eyes on your (genomic) data
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Sep 9, 2020 - JavaScript
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While currently not used in the field (AFAIK) might be worth including bcftools stats for getting statistics on VCF files from genotyping. This would help for genotyping assessiment when not using MultiVCFAnalyzer (which is only really used in aDNA pathogen work).
It would be a simple process, with input channel being VCFs and