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Table 1 Summary of sequence read alignments to the reference genome

From: RNA-Seq analysis uncovers transcriptomic variations between morphologically similar in vivo- and in vitro-derived bovine blastocysts

Sample

In vitro embryos

In vivo embryos

Pair end reads

26,906,451 x 2

38,184,547 x 2

Total sequenced fragments

26,906,451

38,184,547

Total mapped fragments

22,428,488

32,384,577

Uniquely mapped fragments

20,389,330

29,728,363

Fragments mapped to autosomes and X chromosome

19,556,926

28,362,794

Fragments mapped to annotated genes

13,304,981

16,976,922

Fragments mapped to annotated exons

6,942,761

8,185,094

Fragments overlapped with annotated introns

6,362,220

8,791,828