#10 · Transcriptomics
New isoform quantification methods reduce mapping ambiguity and are benchmarked against…
The dominant thread is improving transcript-level quantification and isoform resolution. GaussF is alignment-free, uses GC-stratified k-mer Gaussian CDF self-benchmarking, and is compared against Kallisto and Salmon. A minimal-sharing k-mer strategy isolates transcript-specific regions to reduce mapping ambiguity. CALMeR conditions long-read MAPQ filtering on transcript context with zero-one inflated beta regression, improving spike-in transcript recovery over fixed thresholds. IG-28 identifies high-confidence isoforms from bulk and single-cell full-length cDNA and reports outperforming other tools in benchmarks. Related long-read work extends downstream: DirectClean handles ONT direct-cDNA artifacts, SQANTI-evidence annotates unannotated genomes, and LRP2 adds mass-spectrometry evidence for protein isoforms. Other items, including tWhEEL, Edi-Set-Flow and the mitochondrial RNA tool, address narrower questions.
Published papers
LRP2: a proteogenomics pipeline for long-read informed protein isoform analysis and discovery.
LRP2 is a modular Nextflow pipeline integrating long-read isoform discovery, ORF prediction, differential isoform usage, and DDA/DIA mass-spec evidence for…
tModBase v2.0: an expanded database of tRNA modifications with an AI-powered assistant.
tModBase v2.0 expands a tRNA modification database to 528 datasets across 23 species, adding direct-RNA and modification-specific sequencing data plus an…
DirectClean: artifact-aware preprocessing and read rescue for Oxford Nanopore direct-cDNA transcriptome sequencing.
DirectClean: an artifact-aware preprocessing and read-rescue tool for ONT direct-cDNA reads that handles chimeras and splits recoverable reads; retains more…
Preprints
IG-28 enables identification and quantification of high-confidence isoforms from large bulk and single-cell full-length cDNA datasets
IG-28 is a lightweight isoform identification tool for large bulk and single-cell full-length cDNA datasets, outperforming other tools in benchmarks.
Transcript quantification using context-aware MAPQ modeling
CALMeR conditions long-read MAPQ filtering on transcript context using zero-one inflated beta regression, improving spike-in transcript recovery versus fixed…
tWhEEL: a transcript-aware workflow for quantifying CRISPR knockout feasibility using transcriptome assembly
tWhEEL is a transcript-aware pipeline that infers gene redundancy from transcripts, pairs it with CRISPR guide designs, and scores knockout feasibility across…
GaussF: An Unbiased Gaussian Framework for High-Precision Transcript Quantification with a Programmable Self-Benchmark Model
GaussF is an alignment-free isoform quantification method using GC-stratified k-mer Gaussian CDF self-benchmarking, benchmarked against Kallisto, Salmon,…
Refining RNA-Seq Transcriptome Profiles with Transcript-Specific Minimal-Shared Regions
Proposes a minimal-sharing k-mer strategy that isolates transcript-specific regions to reduce mapping ambiguity in RNA-seq isoform quantification,…
A new tool for quantifying mitochondrial RNA processing intermediates reveals increased levels of immature mRNA species under oxidative stress
New tool quantifies immature mitochondrial mRNAs in short-read RNA-seq; 5' tRNA-extended forms rise under oxidative stress.
SQANTI-evidence: isoform-resolved, evidence-tiered structural annotation of unannotated genomes from long-read RNA-seq
SQANTI-evidence annotates unannotated genomes from long-read RNA-seq alone, using SQANTI3-curated isoforms plus AUGUSTUS predictions; benchmarks show higher…
Edi-Set-Flow: detecting differential RNA-editing at scale
Edi-Set-Flow is a Nextflow pipeline with an R package for transcriptome-wide A-to-I RNA editing detection and differential analysis from bulk RNA-seq, applied…
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