Evidence map›Paper›PMID 41028964›Full record

ArticleBioinformatics (Oxford, England)2022

Full-length isoform constructor (FLIC) - a tool for isoform discovery based on long reads.

Alexandra M Kasianova, Anna V Klepikova, Oleg A Gusev, Guzel R Gazizova, Maria D Logacheva, Aleksey A Penin

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2022. 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
–field-weighted citation impact
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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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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

6 authors.

Alexandra M KasianovaCenter of Molecular and Cellular Biology, Moscow, 119991, Russia.
Anna V KlepikovaLaboratory of Plant Genomics, Vavilov Institute of General Genetics of the Russian Academy of Sciences, Moscow, 119991, Russia.
Oleg A GusevIntractable Disease Research Center, Juntendo University, Tokyo, 113-8421, Japan.
Guzel R GazizovaRegulatory Genomics Research Center, Institute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, 420008, Russia.
Maria D LogachevaCenter of Molecular and Cellular Biology, Moscow, 119991, Russia.
Aleksey A PeninLaboratory of Plant Genomics, Vavilov Institute of General Genetics of the Russian Academy of Sciences, Moscow, 119991, Russia.ORCID 0000-0002-9057-3974

Funding

Ministry of Science and Higher Education
6 · The paper itself

Abstract

motivationAdvances in high-throughput sequencing have illuminated the complexity of transcriptome landscape in eukaryotes. An inherent part of this complexity is the presence of multiple isoforms generated by the alternative splicing and the use of alternative transcription start and polyadenylation sites. However, currently available tools have limited capacity to infer full-length isoforms.

resultsWe developed a new pipeline, FLIC (full-length isoform constructor). FLIC is based on the long-read transcriptome data and integrates several key features: (1) utilizing biological replicate concordance to filter out noise and artifacts; (2) employing peak calling to precisely identify transcription start and polyadenylation sites; (3) enabling robust isoform reconstruction with minimal reliance on existing annotations. We evaluated FLIC using a dedicated set of real and simulated data of Arabidopsis thaliana cDNA sequencing. Results demonstrate that FLIC accurately reconstructs known and novel isoforms, outperforming existing tools, especially in the absence of reference annotations. A direct comparison with CAGE, currently regarded as the gold standard for transcription start site identification, shows that FLIC is equally accurate, while being much less time-consuming. Thus, FLIC provides a valuable tool for comprehensive transcript characterization, particularly for non-model organisms or when dealing with incomplete or inaccurate annotations. AVAILABILITY AND IMPLEMENTATION: FLIC is available at https://github.com/albidgy/FLIC.

Identifiers

PMID41028964
PMCPMC12771368

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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.