When I downloaded a public scRNA dataset(SRX8492075) from the article 'Molecular architecture of the developing mouse brain', why the layout is 'single'?
Anyway, I downloaded it.Then fasterq-dump, I only got one fastq file.
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updated 19 months ago by
Ram
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written 2.5 years ago by
soda
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Hey,
I am also doing this bamtofastq to convert the bam files to fastq file due to the SRA files problem. So, after the bamtofastq, I also have something like what you had:
My question is that if my data is pair end and I ran cellranger on all of these files, and it is errors free using cellranger, can I be sure I did everything correctly with this? based on your SRR number, I also have a feeling that I am using the same dataset as you did.
I solved this problem with the help from a Senior Scientist(10x Genomics).
Thanks a lot!
The senior scientist said:'
Since many of the public archives like SRA do not accept FASTQ files from our version 1 chemistry because the barcode is on an index read, you can download the bam file in SRA directly and convert the bam to fastq.'
1.Get the bam file in SRA
Convert the bam file to fastq
Download 10x bamtofastq from here and use the following command line to convert bam to fastq.
bamtofastq --nthreads=16 inputbam outputfile
After conversion, you can get I1, R1, R2, and R3.
like this:
Hey,
I am also doing this bamtofastq to convert the bam files to fastq file due to the SRA files problem. So, after the bamtofastq, I also have something like what you had:
My question is that if my data is pair end and I ran cellranger on all of these files, and it is errors free using cellranger, can I be sure I did everything correctly with this? based on your SRR number, I also have a feeling that I am using the same dataset as you did.
Best Wishes,
David
Yes you would know if
cellranger
analysis completes properly. There will be a nice html stats file produced if all goes well.