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2.6 years ago
tvibhaps
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10
How to read barcode and umi in 3'v.3.1 10X read1, when GTGGATCAAA+CAGGGTTGGC is same in read 1 and read 2 both? Thanks
Read1
zcat R1.fastq.gz | head -n 10
@A00564:489:HK52WDSX3:3:1101:1362:1000 **1:N:0:GTGGATCAAA+CAGGGTTGGC**
NGCTTGCGTCTAATCGGCAAACCTTAAGAAAAAAAATCAAAAAAAAAAATGGTGTTATGGGTTTATGAGGTCTGCATTACTGGCGCATGTAGGCAAAGACACTCAGCACAACTTGACAAGACAGCGCTCATTTCCAAATCTCTCTCTGAC
+
#:FFFFFFFFFFFFFFFFFFFFFFFFFF,F,FF,FF,,::,,,,F:F,F,,,:,F,,FF::F:F,::F:FF,,F:F:F:,:F,:,:FFF:,,:,F,F:,::,::,,,FF,,:,,,,::F,,::F,::,:FFF,:F:,,,:,:,,,,,,F,
@A00564:489:HK52WDSX3:3:1101:2193:1000 1:N:0:GTGGATCAAA+CAGGGTTGGC
NTGCCTCAGTTTCTTCACTTCGGCTCCAACCAAACAACAATATAAAATTTGTGTGCCACTACCACCAAAATCTTCACCCGCGGCGGCTCCCCCCGGGCCCGCGCCCTCTGCTTCCGAGCTCCCCGCGGCGGCCCACCTACACTGCGCGGC
Read2
zcat R1.fastq.gz | head -n 10
@A00564:489:HK52WDSX3:3:1101:1362:1000 **2:N:0:GTGGATCAAA+CAGGGTTGGC**
CGCGTCTGACTACGGATCAGAAGATTCTAGGTTCGACTCCTGGCAAGCTCGTGCATTTTTTCTATGTCTGAGTGAGATTTGGAAATGAGCGATGTCTTTTCAATTTGTGCTGAGTGTCTTTGCCTACATGCGCCATTAATGCATACCTCA
Can you elaborate what the problem is? R1 contains UMI+CB and R2 contains the cDNA. Specialized software such as CellRanger, STARsolo, kallisto-bustools or alevin will deal with that.
Yes sure! These above are 3' v3.1 10X (Paired-end150bp per sample) R1 and R2 reads.
Check with the 10x documentation. R1 has the CB at 1-16 and UMI at 17-28. That is always the same for v3.
I do not understand. It is paired-end sequencing, I suggest you familiarize yourself with the principle. It is two independent reads but actually for R1 you only need the first 28bp, the rest is meaningless / rubbish.
It's the same. 10x is always paired-end. Read the manual, it will instruct how to read in R1 and R2 with STARsolo.
It's helpful. Thanks