Moderator: Dan D
Dan D ♦ 6.5k
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Docendo discimus.
Posts by Dan D
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... If you want to swim in a bottomless sea of sequencing data and have access to a wide variety of interesting projects in the bioinformatics/big data/data science space, this is for you. You'll be working with me on a growing team solving a number of fun challenges with lots of freedom to utilize new ...
written 6 weeks ago by
Dan D ♦ 6.5k
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Comment:
C: Marketing Project Manager
... Hello Sheila.Smaw!
We believe that this post does not fit the main topic of this site.
This is not related to bioinformatics
For this reason we have closed your question. This allows us to keep the site focused
on the topics that the community can help with.
If you disagree please tell us why ...
written 9 weeks ago by
Dan D ♦ 6.5k
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... Hello Sheila.Smaw!
We believe that this post does not fit the main topic of this site.
This position is not bioinformatics-related.
For this reason we have closed your question. This allows us to keep the site focused
on the topics that the community can help with.
If you disagree please tell ...
written 10 weeks ago by
Dan D ♦ 6.5k
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... OK, I ran it and with the default of mismatch of two it found dup rates between 38-42% on a set of four paired-end datasets. After thinking on this for a bit I come back to my core premise: it's entirely possible that these are not duplicates because of the hundreds of millions of input reads and th ...
written 10 weeks ago by
Dan D ♦ 6.5k
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... Oh, right, I didn't address that in my reply. I will give it a try right now. ...
written 10 weeks ago by
Dan D ♦ 6.5k
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... @finswimmer. This is a standard whole-exome library prep with tight insert size distribution around 225. The duplicate rate is showing between 25-30% from the 200X-targeted and 40-45% for the 400X targeted. I'm looking to report an accurate coverage estimate per library which appropriately considers ...
written 10 weeks ago by
Dan D ♦ 6.5k
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... I'm working with some high-depth whole-exome sequencing data. It's paired-end. Some samples are targeted at 200X and others are 400X average read depth across the exome. The duplicate rate is very high after alignment. I suspect a good portion of these marked duplicates are not actual PCR duplicates ...
written 10 weeks ago by
Dan D ♦ 6.5k
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... OK, so let's look at a typical FASTQ read:
@E00777:238:HABCDCCXY:1:1101:7770:2294 1:N:0:AGCGAAC
ACAGTTGTCCAGTGGCAACAAGGACTCAAGAGATAGAAGACTGATATTATGGTATTTTGAACACCAGCTGAAACCCTTAGTGGCCGAATTTGTGCAGGTCT
+
-AAFFJJJJJF7AFJJAJJJJJAFJJJJ--FF-FF- ...
written 11 weeks ago by
Dan D ♦ 6.5k
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Comment:
C: s. pombe alignment
... Can you please post the command lines you used? ...
written 3 months ago by
Dan D ♦ 6.5k
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4
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Comment:
C: IGV command line control
... Have you seen these?
http://software.broadinstitute.org/software/igv/PortCommands
http://software.broadinstitute.org/software/igv/batch ...
written 4 months ago by
Dan D ♦ 6.5k
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