Moderator: Dan D

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Dan D6.3k
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Posts by Dan D

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Answer: A: Picard alignment statistics error
... I think the most likely explanation for the failure is the asterisk in place of the quality scores, which is a result of feeding FASTA data into the upstream alignment process. This is based on @Medhat 's information, the name of the BAM in @mia 's listed command which contains the word "scaffold", ...
written 9 weeks ago by Dan D6.3k
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Comment: C: Picard alignment statistics error
... Hmmm, there are no ASCII-encoded per-base quality scores in the result. I wonder if that's the problem. Here's what a read with those present would look like: ST-E00273:368:H57THCCXY:5:1106:4300:58268 99 chr1 9997 0 151M = 10329 430 ACCCTAACCCTAACCCTAACCCT ...
written 9 weeks ago by Dan D6.3k
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Comment: C: Picard alignment statistics error
... Those are the MAPQ scores for the read. I'm suggesting that the ASCII-encoded Phred quality scores are out of range. I'm basing that on the [source][1], specifically the `collectQualityData` method referenced in the trace. Would you mind posting the output of your command, minus the `cut`? [1]: ...
written 9 weeks ago by Dan D6.3k
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Answer: A: How to upload fasta file to SSH Supercomputer
... You can use SFTP through an FTP client like filezilla. There are command line clients as well but I'm not sure if you prefer command line or not. Use port 22 on the destination host. If you want to transfer over SSH, the `scp` command is what you want. For example, if you're on the host with the F ...
written 3 months ago by Dan D6.3k
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Answer: A: How to split a fastq file into each corresponding sample.fastq?
... The FASTX toolkit is way out of date, but I think [FASTX Barcode Splitter][1] may be what you need. As long as it works with your specific FASTQ format you're all set. [1]: http://hannonlab.cshl.edu/fastx_toolkit/commandline.html#fastx_barcode_splitter_usage ...
written 3 months ago by Dan D6.3k
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Answer: A: Demultiplexing bcl files into fastq files
... Picard has a BCL-to-FASTQ conversion tool that's not quite as robust as Illumina's proprietary tool. It might be worth a shot: https://broadinstitute.github.io/picard/command-line-overview.html#IlluminaBasecallsToFastq ...
written 3 months ago by Dan D6.3k
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Answer: A: Strand colour from BED file in IGV
... Look [here][1] at the third example. You can set a line in the header of your BED file to automatically color by strand. IGV should pick that up IIRC. [1]: http://hgwdev-kord.cse.ucsc.edu/FAQ/FAQformat.html#format1 ...
written 3 months ago by Dan D6.3k
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Answer: A: Is it possible to get VCF from two fastq files without reference genome?
... **No**. Variant calls are based on a reference genome sequence. Technically you could assemble the raw reads into a draft reference and variant call from *that*, but you'll still have to obtain some reference before you can perform variant calling. EDIT: I may be incorrect in the case that you're ...
written 3 months ago by Dan D6.3k
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Answer: A: Custom features in IGV
... The [IGV documentation][1] references the [official spec for GTF2][2]. That spec only allows for the following values: - `CDS` - `start_codon` - `stop_codon` - `exon` Granted, the GTF format is a special-case derivation of GFF so that's why it doesn't allow introns as a feature type. I'd think ...
written 3 months ago by Dan D6.3k
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Answer: A: Is there any software that can highlight or show the paired end reads within .sa
... If you're looking for an interactive visualization app, [Integrative Genomics Viewer][1] from the Broad can highlight many pairs at once. The same holds true for a similar program, [IGB][2]. [1]: http://software.broadinstitute.org/software/igv/ [2]: http://bioviz.org/igb/ ...
written 4 months ago by Dan D6.3k

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