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I am testing Paladin as an alternative to Diamond for 2 main reasons:
pair-end mode
ability to produce bam files
I can successfully produce bam files in single-end mode, but when feeding it data from the NCBI SRA, the read ids don't seem to be paired, and I get this error below.
Is there a way to tell Paladin to take the R1 + R2 reads as they come without checking if the read ids match between the two?
│ [M::writeReadsProtein] Detecting open reading frames... │
│ [M::writeReadsProtein] Detected and translated 79304452 open reading frames in 112455309 sequences │
│ [M::process] Read 3419102 protein sequences (200000116 AA)... │
│ [M::process] Read 3408448 protein sequences (200000094 AA)... │
│ [M::mem_pestat] # candidate unique pairs for (FF, FR, RF, RR): (0, 0, 0, 0) │
│ [M::mem_pestat] skip orientation FF as there are not enough pairs │
│ [M::mem_pestat] skip orientation FR as there are not enough pairs │
│ [M::mem_pestat] skip orientation RF as there are not enough pairs │
│ [M::mem_pestat] skip orientation RR as there are not enough pairs │
│ [mem_sam_pe] paired reads have different names: "0:1:1:SRR7107847.1", "SRR7107847.2" 0 │
│ │
│ [mem_sam_pe] paired reads have different names: "1:2:2:SRR7107847.2", "SRR7107847.9" │
│ │
│ [mem_sam_pe] paired reads have different names: "0:2:2:SRR7107847.1", "SRR7107847.3" │
│ │
│ [W::sam_read1] Parse error at line 20 │
│ [main_samview] truncated file. │
The text was updated successfully, but these errors were encountered:
Hi,
I am testing Paladin as an alternative to Diamond for 2 main reasons:
I can successfully produce bam files in single-end mode, but when feeding it data from the NCBI SRA, the read ids don't seem to be paired, and I get this error below.
Is there a way to tell Paladin to take the R1 + R2 reads as they come without checking if the read ids match between the two?
The text was updated successfully, but these errors were encountered: