Jonas Korlach

Wellcome Sanger Institute — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

66h-index32.9kcitations189works8.52yr avg
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Research Topics

Genomics and Phylogenetic Studies(54), RNA modifications and cancer(29), Epigenetics and DNA Methylation(19), Chromosomal and Genetic Variations(19), Bacteriophages and microbial interactions(19)

Publications188 total

CiFi: accurate long-read chromosome conformation capture with low-input requirements
Nature Communications·2025· 1 citedOpen Access
CiFi: Accurate long-read chromosome conformation capture with low-input requirements
2025· 1 citedOpen Access
Synchronized long-read genome, methylome, epigenome and transcriptome profiling resolve a Mendelian condition
Nature Genetics·2025· 27 citedOpen Access
Monoallelically expressed noncoding RNAs form nucleolar territories on NOR-containing chromosomes and regulate rRNA expression
eLife·2024· 5 citedOpen Access
Synchronized long-read genome, methylome, epigenome, and transcriptome for resolving a Mendelian condition
2023· 7 citedOpen Access
NCTC3000: a century of bacterial strain collecting leads to a rich genomic data resource
Microbial Genomics·2023· 13 citedOpen Access
Abstract LB078: pbfusion: Detecting gene-fusion and other transcriptional abnormalities using PacBio HiFi data
Cancer Research·2023· 4 cited
Method for sequencing nucleic acid molecules
OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information)·2023Open Access
Author response: Monoallelically expressed noncoding RNAs form nucleolar territories on NOR-containing chromosomes and regulate rRNA expression
2022Open Access
Semi-automated assembly of high-quality diploid human reference genomes
Nature·2022· 218 citedOpen Access
Evolution of the ancestral mammalian karyotype and syntenic regions
Proceedings of the National Academy of Sciences·2022· 92 citedOpen Access
Long‐read HiFi sequencing of <i>NUDT15</i> : Phased full‐gene haplotyping and pharmacogenomic allele discovery
Human Mutation·2022· 10 citedOpen Access
Monoallelically-expressed Noncoding RNAs form nucleolar territories on NOR-containing chromosomes and regulate rRNA expression
2022· 1 citedOpen Access
Establishment of local wastewater-based surveillance programmes in response to the spread and infection of COVID-19 – case studies from South Africa, the Netherlands, Turkey and England
IWA Publishing eBooks·2022· 1 cited
Germline mosaicism of a missense variant in <scp> <i>KCNC2</i> </scp> in a multiplex family with autism and epilepsy characterized by long‐read sequencing
American Journal of Medical Genetics Part A·2022· 13 citedOpen Access
The complete sequence of a human genome
Science·2022· 3.1k citedOpen Access
Genomic answers for children: Dynamic analyses of &gt;1000 pediatric rare disease genomes
Genetics in Medicine·2022· 89 citedOpen Access
Africa: sequence 100,000 species to safeguard biodiversity
Nature·2022· 76 citedOpen Access
Automated assembly of high-quality diploid human reference genomes
2022· 22 citedOpen Access
Establishment of local wastewater-based surveillance programmes in response to the spread and infection of COVID-19 – case studies from South Africa, the Netherlands, Turkey and England
Journal of Water and Health·2022· 28 citedOpen Access
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Frequent Co-authors

Tyson A. Clark(14), Stephen W. Turner(13), Matthew Boitano(11), Evan E. Eichler(10), Chen-Shan Chin(9), Khai Luong(9), Mark Chaisson(8), Arang Rhie(7), Erich D. Jarvis(7), David Porubský(7), Aaron M. Wenger(7), Adam M. Phillippy(7), Patrick Marks(6), Kerstin Howe(6), Paul Peluso(5), Mathieu Foquet(5), Sergey Koren(5), Giulio Formenti(5), Tobias Marschall(5), Jonathan Wood(5)