Changes between Version 5 and Version 6 of SOPs/AssemblingRNAseqReads
- Timestamp:
- 09/21/20 16:35:41 (4 years ago)
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SOPs/AssemblingRNAseqReads
v5 v6 65 65 66 66 67 == Cluster sequences with TGICL ==67 == Clustering sequences with TGICL == 68 68 69 70 {{{ 71 TGICL was designed for the assembly of longer transcript fragments like ESTs. 72 It can still be useful for the multi-step assembly of large or heterogeneous transcript fragments. 73 In these cases, short read assemblers can be used as a first step to generate longer contigs (of variable lengths) which can be further assembled with TGICL. 74 }}} 69 TGICL was designed for the assembly of longer transcript fragments like ESTs. 70 It can still be useful for the multi-step assembly of large or heterogeneous transcript fragments. 71 In these cases, short read assemblers can be used as a first step to generate longer contigs (of variable lengths) which can be further assembled with TGICL. 75 72 76 73 {{{ … … 81 78 == Cleaning the assembled sequence == 82 79 80 Short reads should be generally cleaned of vector/linker/primer sequences before assembly. 81 In some cases we may have pre-assembled contigs that can still contain contamination. 83 82 84 83 {{{ 85 Short reads should be generally cleaned of vector/linker/primer sequences before assembly. 86 In some cases we may be pre-assembled contigs that can still contain contamination. 87 88 Sample command: In this example, contig.fa is the output file from above assembly step 89 bsub "seqclean contig.fa -v /nfs/genomes/UniVec/UniVec_Core -o contig_cleaned.fa" 84 # Sample command: In this example, contig.fa is the output file from above assembly step 85 bsub "seqclean contig.fa -v /nfs/genomes/UniVec/UniVec_Core -o contig_cleaned.fa" 90 86 }}} 91 87