BioinformaticsBioinformaticsPeer-reviewed journal article
Snaptron: querying and visualizing splicing across tens of thousands of RNA-seq samples
Christopher WilksiD, Phani Gaddipati, Abhinav NelloreiD, Ben LangmeadiD
- Citations
- 58
- FWCI
- 1.34
- Field percentile
- top 20%
Abstract
As more and larger genomics studies appear, there is a growing need for comprehensive and queryable cross-study summaries. Snaptron is a search engine for summarized RNA sequencing data with a query planner that leverages R-tree, B-tree and inverted indexing strategies to rapidly execute queries over 146 million exon-exon splice junctions from over 70,000 human RNA-seq samples. Queries can be tailored by constraining which junctions and samples to consider. Snaptron can also rank and score junctions according to tissue specificity or other criteria. Further, Snaptron can rank and score samples according to the relative frequency of different splicing patterns. We outline biological questions that can be explored with Snaptron queries, including a study of novel exons in annotated genes, of exonization of repetitive element loci, and of a recently discovered alternative transcription start site for the ALK gene. Web app and documentation are at http://snaptron.cs.jhu.edu. Source code is at https://github.com/ChristopherWilks/snaptron under the MIT license.
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- recount3: summaries and queries for large-scale RNA-seq expression and splicing
Christopher Wilks, Shijie Zheng, … Ben Langmead·Genome biologyPeer-reviewed·Nov 29, 2021
- Human splicing diversity across the Sequence Read Archive
Abhinav Nellore, Andrew E Jaffe, … Jeffrey T Leek·Genome BiologyPeer-reviewed·Dec 30, 2016
- splicekit: a comprehensive toolkit for splicing analysis from short-read RNA-seq
Gregor Rot, Arne Wehling, … Martin Ebeling·bioRxiv·May 25, 2023
- RsQTL: correlation of expressed SNVs with splicing using RNA-sequencing data
Justin Sein, Liam Flinn Spurr, … Anélia Horvath·bioRxiv·Nov 17, 2019
- SplAdder: Identification, quantification and testing of alternative splicing events from RNA-Seq data
Andre Kahles, Cheng Soon Ong, … Gunnar Rätsch·BioinformaticsPeer-reviewed·Jun 15, 2016
- Efficient and accurate detection of splice junctions from RNAseq with Portcullis
Daniel Mapleson, Luca Venturini, … David Swarbreck·GigaSciencePeer-reviewed·Nov 12, 2018