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Paired end reads #7

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rfcohen opened this issue Dec 11, 2020 · 8 comments
Closed

Paired end reads #7

rfcohen opened this issue Dec 11, 2020 · 8 comments

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@rfcohen
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rfcohen commented Dec 11, 2020

How to feed paired end reads into RAPT? It's not clear from he documentation how one feeds paired end reads into RAPT.

Thanks.

@thibaudnis
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You can provide a file of paired-end reads, with the two reads of a pair adjacent to each other in the file (i.e. spot 1 fwd, spot 1 rev, spot 2 fwd, spot 2 rev) . We will add this to the doc shortly. Thanks for pointing out the omission.

@rfcohen
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rfcohen commented Dec 11, 2020 via email

@thibaudnis
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This is not currently supported.

@rfcohen
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rfcohen commented Dec 11, 2020 via email

@thibaudnis
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Yep, thanks for the suggestions!

@buihoangphuc412
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I have 2 files: R1 and R2, I seem like RAPT did not support
./run_rapt_gcp.sh submitfastq gs://buihoangphuc412/VN0211-s_1_1_sequence.qf.fastq.gz gs://buihoangphuc412/VN0211-s_1_2_sequence.qf.fastq.gz -b gs://buihoangphuc412/VN0211 --organism "Helicobacter pylori" --strain "VN0211"

@thibaudnis
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Okay, I see we need to start accepting R1 and R2. In the meantime, there seems to be a number of options out there for combining the two files: interleave-fastq, or reformat.sh in the BBmap suite that may help.

@thibaudnis
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@buihoangphuc412 and @rfcohen: starting with v0.3.0, you can now provide the forward and reverse reads of a run in separate files, and these files can be gzipped. This version of RAPT is also much faster. See announcement for this new release: https://ncbiinsights.ncbi.nlm.nih.gov/2021/02/12/rapt-release/ . Thanks for your feedback!

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3 participants