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, 15:44, 6 December 2014
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− | == First Things First ==
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− | *Helpful reference to many tools:
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− | ** http://infoplatter.wordpress.com/2014/04/06/bioinformaticians-pocket-reference/
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− | *** links to "cheat-sheets", including, Unix, screen, and vi
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− | * Our wiki with some brief description of how to do some basic commands
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− | **http://genome.sph.umich.edu/wiki/Basic_Linux_Intro
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− | * [[Screen Commands]] for commands to use screen (one way to leave your commands running even after you log out)
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| == Goals of This Session == | | == Goals of This Session == |
| Learn how to go from your FASTQ files to generate Aligned BAMs. | | Learn how to go from your FASTQ files to generate Aligned BAMs. |
− | * Practice setting up and running GotCloud on your own. | + | * '''Your samples have already been aligned''', so we will review the steps that were done |
| + | ** Workshop computers don't have enough compute to align everyone's samples during the workshop |
| + | * You will get to take home both the original FASTQs and the aligned BAMs on a USB drive |
| + | ** You will get it by the end of the week if not before - it takes a while to copy 74G-111G. |
| + | ** 4 samples will get BAMs with "binned" qualities so both FASTQ & BAM would fit on the drive |
| + | *** In future all generated BAMs will be automatically binned. |
| + | ** Those that didn't get sequenced will get a drive with NA12878 public sample on it |
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| {{SeqShopLogin}} | | {{SeqShopLogin}} |