Topic · Molecular Biology · Biochemistry, Genetics and Molecular Biology
Genomics and Phylogenetic Studies
OpenAlex topic; a paper is listed when OpenAlex scores it at least 0.5 for this topic.
1,000+ papers
Twenty-five new microsporidian genomes: Insights into ploidy, reproduction, and the group's pangenome
Amjad Khalaf, Diégo Ayala, Nathan W. Bailey, Lia Bote, Ore Francis, Kamil S. Jaroň, Erna King, Mara Lawniczak, Peter G. Mullin, Kerstin Powers, Thomas O. Powers, Camilla Santos, Mark Blaxter
The paper presents 25 new microsporidian genomes, revealing extreme pangenome diversity and novel tetraploid structures in some species.
bioRxiv · Nov 1, 2026 · PreprintGenomics
DGM Is Dead; Long Live DGM-Star! A Quantization-Theoretic Approach to Gamma Rate Discretization
Roman Sokolovskii, Christoph Stelz, 王雨宁, Ben Bettisworth, Van Nguyen Hoang, SAMUEL J. MARTIN, Thomas Heinis, Oleksiy M. Kozlov, Bùi Quang Minh, Alexandros Stamatakis, Ziheng Yang, Nick Goldman
The paper introduces a new method to discretize Gamma rate distributions in phylogenetics, reducing branch length bias compared to the standard DGM.
bioRxiv · Oct 31, 2026 · PreprintEvolutionary Biology
Fox: Predicting rates of host-symbiont co-evolution events with association-aware attention
Gabriele Di Palma, Laurent Jacob, Catherine Matias, Blerina Sinaimeri
Fox predicts host-symbiont co-evolution event rates directly from sequence alignments without tree reconstruction, achieving high accuracy and speed compared to existing methods.
bioRxiv · Oct 30, 2026 · PreprintBioinformatics
Alignment-Free k-mer Analysis Reveals Age-Associated k-mer Signals in Canine Buccal DNA and Cell-Free DNA
Sonya Hu, Giorgia Del Vecchio, Maciej Długosz, Marek Kokot, Sebastian Deorowicz, Matteo A. Pellegrini
This study identifies age-associated k-mer signals in canine buccal and cell-free DNA using alignment-free k-mer analysis and ridge regression models.
bioRxiv · Oct 30, 2026 · PreprintBioinformatics
Assembly of minimally fragmented metagenomic pangenome graphs
Dylan Duchen, Florencia Martino, Kakhangchung Panmei, Abraham Joseph Kandathil, Steven J. Clipman
The paper introduces PANIMaSTA, a method to construct minimally fragmented metagenomic pangenome graphs for highly diverse viral genomes, improving graph topology for comparative analysis.
bioRxiv · Oct 30, 2026 · PreprintBioinformatics
Towards a complete diploid chicken genome
Shiyu Fan, Jiao Liu, Na Kang, Diyan Li, 李转见, Naiyi Xu, Luohao Xu
This paper presents a nearly complete haplotype-resolved chicken genome using trio-sequencing and long-read data, identifying gaps and structural variants in dot chromosomes.
bioRxiv · Oct 30, 2026 · PreprintGenomics
GaussF: An Unbiased Gaussian Framework for High-Precision Transcript Quantification with a Programmable Self-Benchmark Model
GaussF improves isoform quantification by using a theoretical Gaussian model to correct sequencing biases without empirical data, outperforming existing tools.
bioRxiv · Oct 30, 2026 · PreprintBioinformatics
BaitBench: a comprehensive tool for building, as-sessing, and predicting outcomes for hybrid capture enrichment probes
Aniello M. Infante, Brandon Hollingsworth, Shaun T. Cross
BaitBench is a tool for designing, assessing, and simulating hybrid capture probes, validated with high correlation to real data.
bioRxiv · Oct 30, 2026 · PreprintBioinformatics
IG-28 enables identification and quantification of high-confidence isoforms from large bulk and single-cell full-length cDNA datasets
Alessandro Calicchio, Amanda O. Li, Tanvi Herwadkar, Honey E. Mekonen, Christopher Vollmers
IG-28 identifies and quantifies high-confidence isoforms from large bulk and single-cell full-length cDNA datasets more effectively than existing tools.
bioRxiv · Oct 29, 2026 · PreprintBioinformatics
mito-overview: a mitochondrial report software
Xiaowu Gai, Khushi Ahuja, Élisson Nogueira Lopes
mito-overview integrates mitochondrial coverage, allele fractions, annotations, and read co-occurrence to identify and analyze candidate variants in mitochondrial genomic reports.
bioRxiv · Oct 29, 2026 · PreprintBioinformatics
Creator 1.0: Phylogeny-Guided Stagewise Pretraining for Plant Genome Foundation Models across 1,000 Species
Lin Yang, Sirong Jiang, Yubo Li, Meiling Zou, Yu Xia, Lu Wang, Yingdong Wu, Hao Wang, Wei Xie, Zhiqiang Xia
Creator 1.0 is a plant genome foundation model pretrained on 1,000 species using phylogeny-guided stagewise pretraining, achieving strong performance on plant-related tasks.
bioRxiv · Oct 28, 2026 · PreprintGenomics
A haplotype-resolved, near telomere-to-telomere genome assembly of the desiccation-tolerant plant Vellozia tubiflora
Francine Alves Nogueira de Almeida, Nicholas A. Allsing, Marina Püpke Marone, Mariana Feitosa Cavalheiro, Lucas Eduardo Costa Canesin, Merly Escalona, Oanh Nguyen, Ruta Madhusudan Sahasrabudhe, Diego Mauricio Riaño‐Pachón, Stephen Richards, Harris A. Lewin, Paulo Arruda, Todd P. Michael, Ricardo Augusto Dante, Isabel Rodrigues Gerhardt
This paper presents a near telomere-to-telomere, haplotype-resolved genome assembly of Vellozia tubiflora, a desiccation-tolerant plant, providing genomic resources for evolutionary and comparative studies.
bioRxiv · Oct 28, 2026 · PreprintPlant Biology
Manta and devil ray genome assemblies uncover signatures of pelagic adaptation
Léa Soler-Clavel, Manu Kumar Gundappa, Atlantine Boggio‐Pasqua, Kim Bassos‐Hull, Lisa A. Hoopes, Szu-Hsuan Lee, Marta Ortova Gut, Jessica Gomez Garrido, Fernando Cruz, Tyler Alioto, Tatiana Tilley, Nivesh Jain, Jennifer Balacco, Conor Whelan, Dominic E. Absolon, , Emily Humble
The paper generates high-quality genome assemblies for two manta and devil ray species and identifies structural variations linked to pelagic adaptation.
bioRxiv · Oct 28, 2026 · PreprintEvolutionary Biology
OTTER: Orchestrated Transcriptomic, Tumor-xenograft (PDX/CDX), and Epigenomic Reporting Workflow
Yanhua Zheng, Xin Liu, Yingyu Yi, Xiaojun Sun, Fang Liu, Xiaojing Yan, Cheuk-Him Man, Hongcang Gu, Xiaoxue Wang, Fan Zhang
OTTER improves bisulfite deconvolution in tumor xenograft sequencing by restoring recall to 52%-54% while preserving transcriptomic accuracy.
bioRxiv · Oct 27, 2026 · PreprintBioinformatics
VenusGenome: Genome-Aware Masked Autoencoding for Microbial Genome Representation Learning
Liang Zhang, Yukun Zhang, Yang Tan, Fan Jiang, Bozitao Zhong, Xiaoran Cheng, Liang Hong, Mingchen Li, Yuanxi Yu
VenusGenome improves microbial genome representation learning by using a genome-aware masked autoencoder, achieving high performance in phenotype prediction and gene-level tasks.
bioRxiv · Oct 27, 2026 · PreprintBioinformatics
A New Information Theoretic Approach Shows that Mixture Models Outperform Partition Models for Phylogenetic Analyses of Amino Acid Data
Huaiyan Ren, Changsen Jiang, Thomas K. F. Wong, Yutong Shao, Edward Susko, Bùi Quang Minh, Robert Lanfear
The paper compares mixture and partition models for phylogenetic analyses using the mAIC and finds mixture models consistently outperform partition models.
bioRxiv · Oct 26, 2026 · PreprintEvolutionary Biology
ONT-LibQC: rapid quality control of chromatin assay libraries using shallow nanopore sequencing
ONT-LibQC uses shallow nanopore sequencing to rapidly assess chromatin assay library quality before deep sequencing, showing consistent results with Illumina sequencing.
bioRxiv · Oct 24, 2026 · PreprintGenomics
Two opposite failure modes in alignment-based conservation scores, one inflating and one concealing constraint, are computable before the score is used
The paper identifies two opposite failure modes in alignment-based conservation scores and shows how to correct them to improve score accuracy.
bioRxiv · Oct 24, 2026 · PreprintBioinformatics
Clean Breaks: Attention Force Field Deconvolution of Recombination Across Sequence Manifolds
Sergei L. Kosakovsky Pond, Danielle Callan, Steven Weaver, Hannah Verdonk, Jordan Zehr, Anton Nekrutenko, Taylor K. Paisie, Darren Patrick Martin
RhizAeon deconvolves reticulate evolution by analyzing sequence mosaics and detecting recombination breakpoints with high accuracy and efficiency.
bioRxiv · Oct 23, 2026 · PreprintEvolutionary Biology
Estimating Gene Prevalence with Incomplete Genomes: Application to the Prochlorococcus Pangenome
Stephen Blaskowski, Louis Goldwater Christie, Yubin Raut, Jed A. Fuhrman, Jacob Bien, E. Virginia Armbrust
The paper develops a maximum-likelihood framework to estimate gene prevalence from incomplete genomes and applies it to Prochlorococcus, revealing a pangenome dominated by rare genes.
bioRxiv · Oct 23, 2026 · PreprintMicrobiology
Cuticulome.org: a centralized database of proteins in arthropod cuticles
Alex Wardale, Naomi Nakayama, Cédric Finet
Cuticulome.org provides a curated database of arthropod cuticle proteins with standardized nomenclature and tools for sequence analysis and dataset customization.
bioRxiv · Oct 23, 2026 · PreprintBioinformatics
Described eukaryotic species in published species-level phylogenies: placement by molecular data, dates and date uncertainty
The paper analyzes published eukaryotic phylogenies to assess molecular placement, dating, and uncertainty across species groups.
bioRxiv · Oct 22, 2026 · PreprintEvolutionary Biology
Panagram reveals pangenome architectures underlying trait variation in plants and animals
Katharine M. Jenike, Nicole L. Brown, Sam Kovaka, Delphine Larivière, Robin Burns, Frances L. Chen, Hagai Shohat, Matthias Benoit, Tyler C. Collins, Rachel F. Daniels, Blaine Fitzgerald, Iacopo Gentile, Anat Hendelman, Rachel A. Johnston, Betty Y.H. Huang, , Michael C. Schatz
Alignment-free pan-k-mer profiles track minimap2 similarity (whole-chromosome r^2 0.959-0.968), profile 605 vertebrate genomes in about a day on 40 cores, and nominate trait-linked loci across plants and animals.
bioRxiv · Oct 22, 2026 · PreprintGenomics✦ In-depth digest
G-ALN: a GPU-accelerated BWA-aln algorithm for palaeogenomics
Muhammad Bilal Sharif, Krister Hedfors, Tom van der Valk, Peter D. Heintzman, Love Dalén
G-ALN accelerates BWA-aln for ancient DNA analysis using GPU, achieving faster indexing and alignment speeds with identical output.
bioRxiv · Oct 21, 2026 · PreprintBioinformatics
T2G: fast and accurate transcriptome to genome BAM liftover for short and long read RNA sequencing
Danielle L. Rudler, Shafi Mahmud, Alice Cleynen, Nikolay E. Shirokikh
T2G converts transcriptome-aligned BAM files to genome coordinates, improving specificity and splice junction accuracy across RNA sequencing technologies.
bioRxiv · Oct 21, 2026 · PreprintBioinformatics
Differential sensitivity of k-mer based identification tools using closely related database sequences affects relative abundance estimation
Annie J. Forster, Michael Payne, Rebecca J. Rockett, Cameron Ewart Webb, Tanya Golubchik
This study evaluates how k-mer based tools affect abundance estimation in metagenomic data with closely related references, showing differential performance based on sample-reference distance and reference similarity.
bioRxiv · Oct 21, 2026 · PreprintBioinformatics
Reference mapping and whole-genome alignment yield comparable phylogenomic inferences
Michael V. Westbury, David Alejandro Duchêne
The paper compares phylogenomic inferences from reference mapping and whole-genome alignment across Ursidae species, finding comparable results despite sequence loss.
bioRxiv · Oct 21, 2026 · PreprintEvolutionary Biology