- Mar 25, 2020
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mariabernard authored
1000RNASeq calling : bug fix in script/trimgalore_summary.py when sample are all single end sequenced
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Maria Bernard authored
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- Mar 23, 2020
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mariabernard authored
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mariabernard authored
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Maria Bernard authored
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Maria Bernard authored
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- Mar 13, 2020
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Maria Bernard authored
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Maria Bernard authored
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Maria Bernard authored
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Maria Bernard authored
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- Nov 25, 2019
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Celine Noirot authored
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- Oct 04, 2019
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mariabernard authored
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mariabernard authored
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- Sep 11, 2019
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mariabernard authored
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mariabernard authored
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mariabernard authored
1000RNASeq ASE : add function to call_rate_filter.py, to split genotype and allelel depth by group in TSV files
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- Aug 28, 2019
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Maria Bernard authored
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Maria Bernard authored
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Maria Bernard authored
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Maria Bernard authored
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Maria Bernard authored
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Maria Bernard authored
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- Aug 27, 2019
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mariabernard authored
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mariabernard authored
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- Aug 26, 2019
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mariabernard authored
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mariabernard authored
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mariabernard authored
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mariabernard authored
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mariabernard authored
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mariabernard authored
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- Aug 23, 2019
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mariabernard authored
1000RNASeq ASE: add summary statistics for vcf filtering and add vcf index as input in variantFiltration
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mariabernard authored
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mariabernard authored
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mariabernard authored
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mariabernard authored
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- Aug 22, 2019
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Maria Bernard authored
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Maria Bernard authored
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- Aug 21, 2019
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mariabernard authored
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mariabernard authored
1000RNASeq ASE: change variant filtration results directories and remove var wildcards (only work on SNP)
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mariabernard authored
1000RNASeq ASE: change variant filtration results directories and remove var wildcards (only work on SNP)
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