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Pinned

  1. small RNA analysis from NGS data

    HTML 25 15

  2. analyze isomiRs from seqbuster tool

    R 4 1

  3. Forked from bcbio/bcbio-nextgen

    Validated, scalable, community developed variant calling and RNA-seq analysis

    Python 2 1

  4. Forked from ewels/MultiQC

    Aggregate results from bioinformatics analyses across many samples into a single report.

    Python 1

  5. Forked from chapmanb/cloudbiolinux

    CloudBioLinux: configure virtual (or real) machines with tools for biological analyses

    Python

  6. Create a cromphensive report of DEG list coming from any analysis of RNAseq data

    R 8 6

955 contributions in the last year

Aug Sep Oct Nov Dec Jan Feb Mar Apr May Jun Jul Aug Mon Wed Fri

Contribution activity

August 2019

Created a pull request in HelenaLC/muscat that received 3 comments

accept sce with no cells in some samples

Hi, I ran into errors when the number of samples with cells in a giving cluster was 0. The creation of single cell experiment object will fail sinc…

+26 −3 3 comments

Created an issue in friedlanderlab/mirtrace that received 4 comments

is possible to skip the adapter trimming?

Hi, thanks for the awesome tool :) I am adapting this tool to some pipelines, it is possible to skip the adapter trimming step, for instance, if yo…

4 comments

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