The mapping values and averages for three sheep heart transcriptome experiments were built into a de novo assembly using Trinity and annotated with Trinotate. Reads were mapped to the assembly using S
This file contains both forward (t1-UNIS_S1_L001_R1_001.fastq) and reverse (t1-UNIS_S1_L001_R2_001.fastq) Illumina read data and associated barcode mapping files. In Mapfile_T1 forward primer is linke
*Q20 percentage: Percentage of nucleotide error rate under 0.01. **N: Uncertain base in the output sequencing data. ***N50: Median length of all contigs or unigenes.
