Evidence map›Paper›PMID 22971325›Full record

ArticleGenomics2012

RCDA: a highly sensitive and specific alternatively spliced transcript assembly tool featuring upstream consecutive exon structures.

Xiaolu H Sturgeon, Katheleen J Gardiner

Open access · greenAbstract read
In one paragraph

Article in Genomics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 49% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Xiaolu H SturgeonDepartment of Pediatrics, Linda Crnic Institute for Down Syndrome, University of Colorado Denver, Mail Stop 8608, 12700 E. 19th Avenue, Aurora, CO 80045, USA. Xiaolu.sturgeon@colorado.edu
Katheleen J Gardiner
University of Colorado Denver · US

Funding

Systems Biology for Studies of Cognition in Down SyndromeR01HD056235 · NICHD · UNIVERSITY OF COLORADO DENVER · PI GARDINER, KATHELEEN · 2008 to 2012
$2.7M
NICHD NIH HHS HD056235NICHD NIH HHS R01 HD056235
6 · The paper itself

Abstract

When applied to complex transcript datasets, current tools for automated assembly of mRNA sequences require long run times and produce exponentially increasing numbers of splice variants. Here, we describe RCDA, a genome-based transcript assembly tool comprising RCluster, that recursively clusters transcripts, and DAssemble, that generates composite transcript sequences through path-finding using a directed acyclic graph. Each exon included in a final transcript is associated with an array of all upstream consecutive exon structures obtained from original transcripts. When a depth-first-search path reaches an exon, the path is retained only if it contains a structure from that exon's array. RCDA assemblies, therefore, include only those transcripts with experimentally supported exon patterns. When applied to >23,000 transcripts from human chromosome 21, using biologically reasonable filters, RCDA execution time was approximately 4h. RCDA outperformed ECgene in reconstructing RefSeq transcripts and in limiting the total number of transcripts and transcripts per gene.

Indexed as

Alternative SplicingExonsSoftwareChromosomes, Human, Pair 21Cluster AnalysisGenome, HumanHumansRNA, MessengerSensitivity and SpecificitySequence Analysis, RNARNA, Messenger

Identifiers

PMID22971325
PMCPMC5470730
OpenAlexW1976980844

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.