[Transdecoder-users] Transdecoder help: failure to output final .pep files
Extracting likely coding regions from transcript sequences
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From: Edward G. <e.g...@im...> - 2014-05-12 04:00:10
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Hello I've been trying to run Transdecoder with pfam searching on transcriptome assemblies that I made using Soapdenovo-Trans(SdT). With different assemblies and different PBS parameters (like where I place the data on our system's parallel shared file system etc), Transdecoder creates the temp directory with some of the intermediate files. No finished output files are ever produced. Once I got the .dat file with the pfam hits for my assembly but there were no final .pep .gff3 .cds or .bed files produced and stored anywhere. Am I missing something? Unlike Trinity, SdT plugs in Ns if there is an expected gap between the fragments of a transcript. Could these Ns be tripping up Transdecoder? NOTES: My scripts load the modules our system operators made for Transdecoder and hmmer before sending commands for Transdecoder. These are example entries from my input fasta: >centroid=Fi49merScaf_11503;seqs=3; AACTAAGGGTTTGTTGCTTTTATCAGCGAAATATATTAATGTTTTTAAATTATAGTTGACAACTTTACCGATGAACTATTGAGGTACAGCTTTTTGGGAACATATAGTCTAGTGCCAAGTCCTTCTAGTGCTTTCACACACTCGGCAATACTCTCTTCACTATCAATGTCCATGTTCCAAATTGCCGC... >centroid=Fi49merScaf_29126;seqs=1; TTGGCTGAGAGAACTTACACAAGCCACTTATCGAGCTTCTGCCCCTCCGCCCATCAACATACTTGGAGAACTAAGCAATGATGTAGCGGAAACTGCTGAACCTAGAGCTGTAAATGCTAGGACAGCGGATCTTGTTGTTAATGGAACACTGATTGAGATGAAGTTATCATTATATGTGAAGG... centroid=Fi49merScaf_29118;seqs=1; CTGACATGTGACTGGAGTTCAGACGTGTGCTCTTCCGATCTAGCAAATAGACTGTACAGCATTATAGACAGGTACCTCACAGACTTAAAAAGCCCTTAAGACTGTTTTCCTGTAAAAGAATCTCCTTTTTTAACACAGAAATTATCTACAAAATCTAATTCGGAGACCACGGTGTTAACCAAATC... Thanks Ed Dr. Edward K Gilding The Institute of Molecular Biosciences The University of Queensland Brisbane, QLD 4072 Australia O: +61 07 3346 2014 |