- 09 May, 2018 1 commit
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Blaise Li authored
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- 24 Apr, 2018 1 commit
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Blaise Li authored
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- 12 Apr, 2018 1 commit
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Blaise Li authored
Also introduced minor modification recently made for other pipelines.
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- 23 Mar, 2018 1 commit
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Blaise Li authored
Currently only the folds computed by DESeq2 are available for RNA-seq.
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- 12 Mar, 2018 1 commit
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Blaise Li authored
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- 08 Mar, 2018 1 commit
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Blaise Li authored
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- 05 Mar, 2018 1 commit
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Blaise Li authored
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- 28 Feb, 2018 1 commit
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Blaise Li authored
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- 21 Feb, 2018 1 commit
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Blaise Li authored
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- 08 Feb, 2018 1 commit
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Blaise Li authored
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- 22 Jan, 2018 1 commit
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Blaise Li authored
Made paired scatterplot plotting function part of libhts as `plot_paired_scatters`. Modifications in small RNA-seq pipeline not tested.
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- 16 Jan, 2018 1 commit
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Blaise Li authored
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- 12 Jan, 2018 1 commit
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Blaise Li authored
The genome is now configurable. This lead to large modifications in the config file. Output organization simplified.
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- 18 Dec, 2017 2 commits
- 14 Dec, 2017 1 commit
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Blaise Li authored
This makes the DE results easier to compare with those from small RNA-seq.
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- 12 Dec, 2017 1 commit
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Blaise Li authored
For RNA-seq and GRO-seq, log and data directories are now subdirectories of output directories. local_annot_dir also moves as subdirectory of GRO-seq output.
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- 08 Dec, 2017 1 commit
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Blaise Li authored
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- 06 Dec, 2017 4 commits
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Blaise Li authored
This seems to happen on data matrices with only 2 rows left after filtering.
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Blaise Li authored
The goal is to be able to factorize the rule in a wrapper.
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Blaise Li authored
Started to apply to RNA-seq and GRO-seq technique used in small RNA-seq.
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Blaise Li authored
I should check to be sure that this is the correct thing to do. The other possibility would be to sum using agg: https://stackoverflow.com/a/35403903/1878788
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- 20 Oct, 2017 1 commit
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Blaise Li authored
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- 17 Oct, 2017 1 commit
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Blaise Li authored
lfcMLE may bring problems with low-expressed genes. Also: - Boxplots with labels turned 90 degrees - do_deseq2 returns size factors
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- 15 Sep, 2017 1 commit
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Blaise Li authored
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- 12 Sep, 2017 1 commit
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Blaise Li authored
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- 11 Sep, 2017 1 commit
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Blaise Li authored
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- 07 Sep, 2017 1 commit
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Blaise Li authored
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- 06 Sep, 2017 1 commit
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Blaise Li authored
It currently fails when libraries have too many rRNA reads: https://github.com/arq5x/bedtools2/issues/565 Also added lfc distribution and improved MA plot.
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- 09 Aug, 2017 1 commit
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Blaise Li authored
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- 28 Jul, 2017 1 commit
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Blaise Li authored
Also moved save_plot to libworkflows.
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- 27 Jul, 2017 1 commit
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Blaise Li authored
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- 26 Jul, 2017 1 commit
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Blaise Li authored
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- 24 Jul, 2017 2 commits
- 21 Jul, 2017 2 commits
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Blaise Li authored
The column was only added later, when grouping the results with the counts.
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Blaise Li authored
Library standedness was not taken into account correctly, and too many reads in repeated regions were discarded in featureCounts: <https://bioinformatics.stackexchange.com/q/2101/292> Also added mean across replicates for bigwig files and use various log fold change thresholds to classify genes.
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- 17 Jul, 2017 1 commit
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Blaise Li authored
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- 06 Jul, 2017 1 commit
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Blaise Li authored
The normalization for the bigwig files is currently based on reads forward-mapping on protein-coding genes. Bigwig file generation uses a new method implemented in bam2bigwig.sh which is faster than bamCoverage from deeptools. It generates slightly different results (see c5bbd282) and has not been tested for compatibility with further deeptools-based analyses..
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- 29 Jun, 2017 1 commit
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Blaise Li authored
Also fixed missing pandas import in libworkflows.
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