Jean Monlong
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jmonlong.bsky.social
Jean Monlong
@jmonlong.bsky.social
Human genomics researcher at INSERM in Toulouse, France
Structural variant, pangenomes
https://jmonlong.github.io/
Reposted by Jean Monlong
🦒Long read giraffe is out!🦒
Mapping long reads to pangenome graphs is ~10x faster than with GraphAligner, with veeery slightly better mapping accuracy, short variant calling, and SV genotyping than GraphAligner or Minimap2
Rapid, accurate long- and short-read mapping to large pangenome graphs with vg Giraffe https://www.biorxiv.org/content/10.1101/2025.09.29.678807v1
October 2, 2025 at 6:28 AM
Reposted by Jean Monlong
New tgv release: local cache!

tgv download hg38

Download UCSC reference genomes to a local sqlite db for much faster browsing. Awesome Rust tools (twobit, bigtools) made this simple.

github.com/zeqianli/tgv
GitHub - zeqianli/tgv: Explore 5,000+ genomes in the terminal. Light, blazing fast 🚀, vim-motion.
Explore 5,000+ genomes in the terminal. Light, blazing fast 🚀, vim-motion. - zeqianli/tgv
github.com
July 19, 2025 at 11:37 PM
Reposted by Jean Monlong
New figure for my thesis showing why Giraffe is the best long read pangenome mapper. No further evidence will be provided.
February 14, 2025 at 7:45 PM
Reposted by Jean Monlong
A couple of months ago I tried the @peercommunityin.bsky.social publishing system & I can only recommend it (pun intended). Please see below to change how we publish science 1/n
January 31, 2025 at 10:36 AM
Reposted by Jean Monlong
Researchers at @ucsantacruz.bsky.social have demonstrated how long-read sequencing could improve detection of diseases that have eluded diagnosis, at a fraction of the cost. New clinical tests could be on the way.
🗞 news.ucsc.edu/2025/01/pate...
👏🏼👏🏿👏🏾 @khmiga.bsky.social @benedictpaten.bsky.social
January 24, 2025 at 7:17 PM
Reposted by Jean Monlong
Organising the EMGM in Brest next year: emgm2025.sciencesconf.org
53rd European Mathematical Genetics Meeting - Sciencesconf.org
emgm2025.sciencesconf.org
November 29, 2024 at 8:54 PM
Reposted by Jean Monlong
Hurray for cats (and regulatory mutations)
November 29, 2024 at 7:41 AM
Reposted by Jean Monlong
"We engineered approximately 45,000 insertions, 6,000 deletions and 41,000 amino acid substitutions across the nearly 2,200 coding positions of the Enterovirus A71 proteome, quantifying their effects on viral fitness"
www.nature.com/articles/s41...
Deep mutation, insertion and deletion scanning across the Enterovirus A proteome reveals constraints shaping viral evolution - Nature Microbiology
Deep mutational scanning of Enterovirus A71 maps and quantifies the impact of genomic insertions, deletions and substitutions on virus fitness and highlights the role of insertions and deletions in th...
www.nature.com
November 28, 2024 at 6:27 PM
Reposted by Jean Monlong
40 years later, and we still don't have a good answer. (original article is quite fun: www.jstor.org/stable/24084...)
November 26, 2024 at 8:29 AM
Reposted by Jean Monlong
1/ 🧵 Free resources for scientists

💡 Covering research skills, careers, #SciComm, leadership, activism and more, everything in this thread appears on our Learning Resources page, with tips for researchers and academics at any career stage. #AcademicChatter #ECRChat
https://buff.ly/4f8vIpk
Learning resources for scientists · eLife
A collections of articles that provide practical resources and guidance for researchers and academics
buff.ly
November 26, 2024 at 3:42 PM
Reposted by Jean Monlong
🎨 In case anyone need…

The NIH BioArt Source is an awesome library of *free* professionally drawn illustrations for scientific presentations or figures. Downloadable in HD. Thank you NIH for this invaluable tool 🙏!

Check it out 👇
bioart.niaid.nih.gov
November 23, 2024 at 3:50 PM
Reposted by Jean Monlong
🧬🔍There are 50 petabases of freely-available DNA sequencing data. We introducing Logan Search which allows you to search for any DNA sequence in minutes, bringing Earth’s largest genomic resource to your fingertips.
🏔️ logan-search.org 🏔️
#Genomics #Bioinformatics #OpenScience
November 11, 2024 at 7:29 PM
Reposted by Jean Monlong
We have a method for fast GWAS data access. STABIX adds a p-value index that with a position index (what TABIX has) allows you to quickly retrieve, eg. all significant SNPs in a target gene. Also column compression to reduce the size. www.biorxiv.org/content/10.1...

github.com/kristen-schn...
STABIX: Summary statistic-based GWAS indexing and compression
Genome-Wide Association Studies (GWAS) are widely used to investigate the role of genetics in disease traits, but the resulting file sizes from these studies are large, posing barriers to efficient st...
www.biorxiv.org
November 21, 2024 at 3:11 PM
Reposted by Jean Monlong
📣 Preprint alert! We have studied the formation of pair-wise and multi-way enhancer-promoter interactions in the #3Dgenome in a lymphoid-to-myeloid transdifferentiation system and learned interesting new things about their function in #GeneRegulation. 1/10
www.biorxiv.org/content/10.1...
www.biorxiv.org
November 22, 2024 at 11:58 AM