Evidence map›Paper›PMID 42834519›Full record

ArticleBioinformatics (Oxford, England)2026

MAJEC: unified gene, isoform, and locus-level transposable element quantification from RNA-seq.

Tian-Yeh Lim, Ari J Firestone

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Tian-Yeh LimCalico Life Sciences LLC, South San Francisco, CA 94080, United States.
Ari J FirestoneCalico Life Sciences LLC, South San Francisco, CA 94080, United States.ORCID 0000-0001-9902-443X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationThe study of transposable elements (TEs) has become increasingly central to fields such as cancer biology, immunology, and aging. Accurately quantifying disease- or laboratory-mediated perturbations in these elements is critical to support this expanding research, yet current RNA-seq pipelines struggle with the pervasive overlap between TEs and protein-coding genes. Existing tools either aggregate to the subfamily level with no locus resolution (TEtranscripts), or provide locus-level quantification without modeling gene overlap (Telescope), with the latter attributing over 40% of TE signal to the 1.1% of loci that overlap gene exons.

resultsWe present Momentum Accelerated Junction Enhanced Counting (MAJEC), a unified Expectation-Maximization (EM) framework that jointly quantifies genes, transcript isoforms, and individual TE loci from BAM alignments in a single pass. Splice junction evidence informs transcript-level priors, enabling MAJEC to probabilistically distinguish genic from TE-derived reads. This approach was independently validated against Salmon and RSEM on isoform quantification benchmarks. The joint feature space reduces exon-overlap contamination of locus-level TE estimates from 43% of total signal (Telescope) to 5% (MAJEC), while preserving subfamily-level accuracy (differential expression r = 0.987 versus TEtranscripts). Using paired biological vignettes, we demonstrate that MAJEC correctly resolves both the false TE reactivation artifacts endemic to TE-only models, and the false gene upregulation artifacts that occur when heuristic rules misassign genuine intragenic TE transcription. MAJEC simultaneously produces the isoform and locus-level resolution that TEtranscripts lacks, with greater accuracy than Telescope, and runs faster than either. AVAILABILITY AND IMPLEMENTATION: MAJEC is available at https://github.com/calico/majec and via PyPI/Bioconda; analysis code and data are deposited at https://doi.org/10.5281/zenodo.19224157.

Indexed as

DNA Transposable ElementsRNA-SeqSequence Analysis, RNASoftwareAnimalsHumansProtein IsoformsDNA Transposable ElementsProtein Isoforms

Identifiers

PMID42834519
PMCPMC13676384

What OpenQuestion holds

Textmetadata
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.