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. 2017 Jun 14;313(3):F585–F595. doi: 10.1152/ajprenal.00228.2017

Table 1.

De novo assembly statistics using different BLASTx alignment cutoffs

Column A; Mammal Filter and e-Value ≤1e−4 Column B: ≥80% of a Swiss-Prot Sequence Matched Column C: ≥40% Swiss-Prot Sequence Covered and ≥70% identity
K3 assembly: 180,731 contigs with BLASTx result
    De novo contigs constructed 46,741 8,055 19,812*
    Swiss-Prot sequences aligned 16,465 4,875 9,510*
    Swiss-Prot Genes 11,895 4,677 8,433*
K10 assembly: 53,511 contigs with BLASTx result
    De novo contigs constructed 26,684 6,478 13,251
    Swiss-Prot sequences aligned 13,005 4,498 8,220
    Swiss-Prot Genes 10,529 4,336 7,576

Contigs generated by the Trinity de novo assembly using minimum kmer coverage settings 3 and 10 were aligned using BLASTx to the Swiss-Prot database. For each assembly the table shows the number of contigs that pass the filter denoted by the column heading, the number of Swiss-Prot sequences aligned by the contigs, and the number of Swiss-Prot genes matched in the assembly. Column A: filter for BLASTx matches to sequences in mammals with an e-value <1e−4. Columns B and C: further filtering of the contigs selected by the mammal and e-value filter. Column B: filter for contigs that match identically to ≥80% of the full sequence found in Swiss-Prot. Column C: filter for contigs that cover ≥40% of the Swiss-Prot sequence as determined using a Trinity module and with ≥70% identity to the sequence as reported by BLAST. Details of these filters can be found in materials and methods.

*

Final assembly chosen for further analysis.