Author

Inger Jonasson

Uppsala University

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:database / resource· 1 Approach:experimental assay· 1 Assay:long-read sequencing· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Adam AmeuriD· 2 shared Ulf B GyllensteniD· 2 shared Andreas KähäriiD· 1 shared Ann‐Christine SyväneniD· 1 shared Åsa JohanssoniD· 1 shared Björn NystedtiD· 1 shared Daniel NilssoniD· 1 shared David GreenbergiD· 1 shared

Activity by Year

2017-2017 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenomics

Adam AmeurORCID

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2 papers

Recent·Most cited

Amplification-free, CRISPR-Cas9 Targeted Enrichment and SMRT Sequencing of Repeat-Expansion Disease Causative Genomic Regions

Yu‐Chih Tsai, David Greenberg, James Powell, Ida Höijer, Adam Ameur, Maya Strahl, Ethan Ellis, Inger Jonasson, Ricardo Mouro Pinto, Vanessa Chantal Wheeler, Melissa Laird Smith, Ulf B Gyllensten, Robert Sebra, Jonas Korlach, Tyson A. Clark

Combining amplification-free CRISPR-Cas9 targeted enrichment with Single Molecule, Real-Time (SMRT) long-read sequencing captures and sequences human repeat-expansion disease loci across HTT, FMR1, C9orf72, and ATXN10 without PCR bias.

bioRxiv · Oct 16, 2017 · PreprintGenomics

SweGen: A whole-genome map of genetic variability in a cross-section of the Swedish population

Adam Ameur, Johan Dahlberg, Pall I. Olason, Francesco Vezzi, Robert Karlsson, Marcel Martin, Johan Viklund, Andreas Kähäri, Pär Lundin, Huiwen Che, Jessada Thutkawkorapin, Jesper Eisfeldt, Samuel Lampa, Mats Dahlberg, Jonas Hagberg, , Ulf B Gyllensten

SweGen provides a high-quality whole-genome map of genetic variation in the Swedish population, useful for clinical genetics and association studies.

European Journal of Human Genetics · Aug 23, 2017Peer-reviewedGenetics