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. Author manuscript; available in PMC: 2014 Feb 1.
Published in final edited form as: Nat Protoc. 2013 Jul 11;8(8):10.1038/nprot.2013.084. doi: 10.1038/nprot.2013.084

Table 1.

Example contents of RSEM’s ‘isoforms.results’ file

transcript_id gene_id length effective_length expected_count TPM FPKM IsoPct
comp56_c0_seq1 comp56_c0 3739 3443 637.65 16664.43 7008.23 11.26
comp56_c0_seq2 comp56_c0 3697 3401 4966.34 131393.38 55257.53 88.74
comp62_c0_seq1 comp62_c0 7194 6898 4551.13 59364.09 24965.59 95.54
comp62_c0_seq2 comp62_c0 7076 6778 208.87 2771.95 1165.74 4.46

Transcript_id: Trinity transcript identifier

Gene_id: Trinity component to which the reconstructed transcript was derived.

Length: length of the reconstructed transcript.

Effective length: The mean number of 5′ start positions from which an RNA-Seq fragment could have been derived from this transcript, given the distribution of fragment lengths inferred by RSEM. The value is equal to (transcript_length - mean_fragment_length + 1).

Expected count: number of expected RNA-Seq fragments assigned to the transcript given maximum likelihood transcript abundance estimates.

TPM: transcripts per million

FPKM: number of RNA-Seq fragments per kilobase of transcript effective length per million fragments mapped to all transcripts.

IsoPct: percent of expression for a given transcript compared to all expression from that Trinity component.