Cellular source and mechanisms of high transcriptome complexity in the mammalian testis (RNA-Seq cells)
Understanding the extent of genomic transcription and its functional relevance is a central goal in genomics research. However, detailed genome‐wide investigations of transcriptome complexities in major mammalian organs and their underlying cellular sources, transcriptional mechanisms, and functional relevance have been scarce. Here we first show, using extensive RNA‐seq data, that transcription of both functional and nonfunctional genomic elements is ...
Provenance — who produced it, who reused it
Linked to 12 papers in the literature. Roles are inferred factual signals (who deposited the data vs who reused it), with counts — never a judgement about any author.
- The conserved RNA helicase YTHDC2 regulates the transition from... 2017 · 213 cites
- An Orchestrated Intron Retention Program in Meiosis Controls Tim... 2017 · 190 cites
- ketu mutant mice uncover an essential meiotic function for the a... 2018 · 160 cites
- Integrated transcriptome analysis of mouse spermatogenesis 2014 · 156 cites
- Alternative cleavage and polyadenylation in spermatogenesis conn... 2016 · 92 cites
- Ptbp2 Controls an Alternative Splicing Network Required for Cell... 2017 · 88 cites
6 further papers cite this accession but reuse could not be confirmed.
Deep data QC
33/100 · FStandardized, field-standard QC computed by touching the data — every metric states how it was obtained · evidence: measured
The F grade is a transparent weighted average. Each metric below scored from 0–100% against the published bulk-RNA-seq thresholds, weighted by its importance; nothing is hidden or subjective.
measured = computed from the data · extrapolated/reported = derived or from the repository · dq-1.0