Genomics - SE Variation
Version 1

Workflow Type: Galaxy

Analysis of variation within individual COVID-19 samples using Illumina Single End data. More info can be found at


ID Name Description Type
0_Input Dataset Collection n/a n/a
  • File
NC_045512 n/a n/a
  • File


ID Name Description
10_Call variants n/a n/a
11_SnpEff eff n/a n/a
12_SnpSift Extract Fields n/a n/a
13_Collapse Collection n/a n/a
2_fastp n/a n/a
3_SnpEff build n/a n/a
4_MultiQC n/a n/a
5_Bowtie2 n/a n/a
6_MultiQC n/a n/a
7_MarkDuplicates n/a n/a
8_MultiQC n/a n/a
9_Realign reads n/a n/a
Total size: 50.7 KB
help Creators and Submitter
  • Dannon Baker
  • Marius van den Beek
  • Dave Bouvier
  • John Chilton
  • Nate Coraor
  • Frederik Coppens
  • Bert Droesbeke
  • Ignacio Eguinoa
  • Simon Gladman
  • Björn Grüning
  • Delphine Larivière
  • Gildas Le Corguillé
  • Andrew Lonie
  • Nicholas Keener
  • Sergei Kosakovsky Pond
  • Wolfgang Maier
  • Anton Nekrutenko
  • James Taylor
  • Steven Weaver

Views: 815   Downloads: 39

Created: 10th Apr 2020 at 13:54

Last used: 19th Jan 2022 at 05:19

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Version History

Version 1 (earliest) Created 10th Apr 2020 at 13:54 by Bert Droesbeke

Added/updated 3 files

Open master 1bd5589

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