wgs
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software for processing tuberculosis whole genome data. interface to the BWA, VarScan, SamTools etc.
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Feb 8, 2017
PySeqArray: data manipulation of whole-genome sequencing variants with SeqArray files in Python (pre-release version)
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Aug 25, 2017 - C++
Converter for Swiss-Coordinates and WGS-Coordinates.
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Apr 29, 2018 - PHP
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May 23, 2018 - Python
De novo SNV analysis pipeline
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Jul 13, 2018 - R
Seave is a web platform that enables genetic variants to be easily filtered and annotated with in silico pathogenicity prediction scores and annotations from popular disease databases. Seave stores genomic variation of all types and sizes, and allows filtering for specific inheritance patterns, quality values, allele frequencies and gene lists. …
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Aug 9, 2018 - HTML
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Dec 31, 2018 - WDL
Associate outliers with rare variation
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Apr 8, 2019 - Python
Kourami: Graph-guided assembly for HLA alleles
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May 21, 2019 - Java
Using Convolutional Neural Networks to model an association between a genomic sequence and the number of sequenced reads that align to it
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Jul 18, 2019 - Jupyter Notebook
Bayesian method for Environmental correlations analysis pipeline
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Oct 10, 2019 - Python
NGS Processing Pipelines for WGS and WES data
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Nov 11, 2019 - Python
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