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Yuichi Shiraishi

@friend1ws.bsky.social

Cheif, Division of Genome Analysis Platform Development, National Cancer Center Research Institute. https://friend1ws.github.io

34 Followers  |  32 Following  |  9 Posts  |  Joined: 25.11.2024
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Posts by Yuichi Shiraishi (@friend1ws.bsky.social)

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Absolutely thrilled to share the latest work from my lab focused on the variation and evolution of human centromeres among global populations! We assembled 2,110 human centromeres, identifying 226 new major haplotypes and 1,870 Ξ±-satellite HOR variants. www.biorxiv.org/content/10.6...

16.12.2025 16:05 β€” πŸ‘ 108    πŸ” 46    πŸ’¬ 4    πŸ“Œ 2
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65 Genomes Expand Our Picture Of Human Genetics Researchers closely examined the genomes of 65 individuals to paint a more complex, and more complete, picture of human genetic diversity.

Complete genomes alert! @glennislogsdon.bsky.social, @christinebeck.bsky.social, and I were on @scifri.bsky.social today talking about "Complex genetic variation in nearly complete human genomes"
πŸ“„ www.nature.com/articles/s41...
πŸ“» www.sciencefriday.com/segments/65-...

01.08.2025 20:49 β€” πŸ‘ 50    πŸ” 16    πŸ’¬ 1    πŸ“Œ 2

This is a highly collaborative effort with outstanding colleagues:
πŸ™ Dr. Seishi Ogawa, @yotarochi.bsky.social, @glennislogsdon.bsky.social, @thinks.lol, Masahiro Sugawa, Yoshitaka Sakamoto, and many others.
We hope this work helps reshape how we study centromere variation and its link to disease.

30.07.2025 13:49 β€” πŸ‘ 2    πŸ” 0    πŸ’¬ 0    πŸ“Œ 0
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Finally, using ascairn, we analyzed 142 TCGA brain tumor whole genomes with 1p/19q co-deletion (class-defining centromere translocation).
We found that these events are dicentric, and that centromere haplogroups may influence the occurence of 1p/19q co-deletion!

30.07.2025 13:49 β€” πŸ‘ 1    πŸ” 0    πŸ’¬ 1    πŸ“Œ 0
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We applied ascairn to over 3,300 WGS samples from the 1000 Genomes Project and Human Genome Diversity Project.
This revealed population-level differences in centromere haplogroups, providing new insights into human ancestry and migration. (4/n)

30.07.2025 13:49 β€” πŸ‘ 1    πŸ” 0    πŸ’¬ 1    πŸ“Œ 0
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GitHub - friend1ws/ascairn: Centromere sequence analysis using rare k-mer markers Centromere sequence analysis using rare k-mer markers - friend1ws/ascairn

We developed a new algorithm, ascairn, to infer centromere haplogroups directly from short-read WGS data.
βœ… Accuracy exceeds 95% for most chromosomes!
The tool is freely available here:
πŸ”— github.com/friend1ws/as...
(3/n)

30.07.2025 13:49 β€” πŸ‘ 1    πŸ” 0    πŸ’¬ 1    πŸ“Œ 0
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We extracted rarely observed short nucleotide sequences (rare k-mers) from centromere assemblies generated by several pangenome consortia.
These rare k-mers act like β€œcentromere SNPs”!
Rare k-mer profiles group centromere sequences into evolutionarily related haplogroups.
(2/n)

30.07.2025 13:49 β€” πŸ‘ 1    πŸ” 0    πŸ’¬ 1    πŸ“Œ 0
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Rare k-mers reveal centromere haplogroups underlying human diversity and cancer translocations Centromeres are among the most diverse and dynamically evolving regions of the human genome and are commonly affected in various human cancers. However, organized into highly repetitive Ξ±-satellite hi...

🚨New preprint out!
🧬Short reads can now decode centromeres.
🌍We reveal population-scale centromere haplogroups and their links to disease.
biorxiv.org/content/10.1... (1/n)

30.07.2025 13:49 β€” πŸ‘ 3    πŸ” 6    πŸ’¬ 1    πŸ“Œ 0
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Systematically developing a registry of splice-site creating variants utilizing massive publicly available transcriptome sequence data - Nature Communications Splice-site creating variants (SSCVs) are considered promising candidates for treatment with antisense oligonucleotides. Here, the authors present a novel framework to screen for SSCVs solely using tr...

SSCVs are genomic variants that create novel splice sites and alter splicing. This updated resource supports variant interpretation and drug target discovery, especially with antisense oligonucleotides.
Details in our paper πŸ‘‰ www.nature.com/articles/s41...

26.07.2025 08:10 β€” πŸ‘ 0    πŸ” 0    πŸ’¬ 0    πŸ“Œ 0
SSCV DB Ver.1.1

🧬 SSCV DB updated!
We screened 525,323 RNA-seq samples (up from 310,699 at the time of our SSCV paper) and identified 48,569 splice-site creating variants (SSCVs).
πŸ‘‰ sscvdb.io

#RNAseq #splicing #ASO

26.07.2025 08:10 β€” πŸ‘ 0    πŸ” 0    πŸ’¬ 1    πŸ“Œ 0

New from the lab by algorithm geek Hajime Suzuki! Genome assembly in centromeric regions is still challenging. By focusing on k-mer periodicity, Hajime implemented a novel hashing approach (github.com/ocxtal/mm2-ivh), which dramatically improves assembly in repetitive regions like centromeres!

18.07.2025 15:07 β€” πŸ‘ 1    πŸ” 0    πŸ’¬ 0    πŸ“Œ 0

Postdoc position opening in my group! Research projects: pangenomes for diverse organisms, genome evolution, biocomputing, language models. Please reach out if interested!

17.07.2025 07:53 β€” πŸ‘ 28    πŸ” 30    πŸ’¬ 1    πŸ“Œ 1
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πŸ“’ HPRC Release 2 is here!

Now with phased genomes from 200+ individuals, a 5x increase from Release 1.

Explore sequencing data, assemblies, annotations & alignments in our interactive data explorer ⬇️:

humanpangenome.org/hprc-data-re...

12.05.2025 13:14 β€” πŸ‘ 37    πŸ” 28    πŸ’¬ 0    πŸ“Œ 3
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The Betrayal of Itō Shiori: When Lawyers Do More Harm Than Good - Unseen Japan Itō Shiori's award-winning documentary BLACK BOX DIARIES still can't be screened in Japan. Is that truly in the interests of justice?

Itō Shiori's award-winning documentary BLACK BOX DIARIES still can't be screened in Japan. A group of lawyers - Itō's former attorneys - say she didn't get permission for some of the footage. But is that true? Why are attorneys undermining their own former client?

20.02.2025 19:31 β€” πŸ‘ 57    πŸ” 21    πŸ’¬ 0    πŸ“Œ 0