IsoSCM

IsoSCM applies change-point analysis to RNA-seq-based transcript assemblies to improve annotation of 3' untranslated regions (3' UTRs) and detection of alternative cleavage and polyadenylation (APA) events.


Key Features:

  • Change-Point Analysis Integration: Integrates change-point analysis to detect transcript termini and partition RNA-seq signal into distinct 3' UTR isoforms.
  • Improved 3' UTR Annotation: Reduces fragmentation of long 3' UTRs and distinguishes tandem isoforms for more accurate 3' end annotation.
  • Alternative Cleavage and Polyadenylation Detection: Identifies APA events by resolving subtle variations in transcript ends indicative of alternative cleavage and polyadenylation.
  • Evaluated Sensitivity and Specificity: Demonstrates superior sensitivity and specificity in annotating 3' termini based on evaluations with simulated and genuine RNA-seq datasets.
  • Support for Genome-Wide APA Analysis: Enables genome-wide investigations of APA and 3' UTR regulation across genes and conditions.

Scientific Applications:

  • Gene Expression Studies: Assess how changes in 3' UTR length and isoform composition affect gene regulation.
  • RNA Processing Research: Investigate mechanisms and consequences of alternative cleavage and polyadenylation (APA).
  • Cellular Identity and Disease Analysis: Examine APA pattern differences related to cellular differentiation, environmental responses, and disease progression.

Methodology:

Performs transcript assembly from RNA-seq data and applies change-point analysis to identify transcript ends and alternative cleavage and polyadenylation (APA) events.

Topics

Details

Tool Type:
command-line tool
Operating Systems:
Linux, Windows
Added:
8/3/2017
Last Updated:
11/25/2024

Operations

Publications

Shenker S, Miura P, Sanfilippo P, Lai EC. IsoSCM: improved and alternative 3′ UTR annotation using multiple change-point inference. RNA. 2014;21(1):14-27. doi:10.1261/rna.046037.114. PMID:25406361. PMCID:PMC4274634.

PMID: 25406361
PMCID: PMC4274634
Funding: - National Institutes of Health: R01-NS074037, R01-NS083833

Documentation

Links