Ida Höijer
1:e Forskningsing vid Institutionen för immunologi, genetik och patologi; Faciliteter; Klinisk genomik Uppsala
- Telefon:
- 018-471 48 21
- Mobiltelefon:
- 073-469 79 13
- E-post:
- ida.hoijer@igp.uu.se
- Besöksadress:
- Dag Hammarskjölds väg 20
751 85 Uppsala - Postadress:
- Rudbecklaboratoriet
751 85 UPPSALA
1:e Forskningsing vid Institutionen för immunologi, genetik och patologi; Faciliteter; Uppsala genomcenter
- Mobiltelefon:
- 073-469 79 13
- Besöksadress:
- BMC, Husargatan 3
75122 Uppsala - Postadress:
- Box 815
75108 Uppsala
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Publikationer
Urval av publikationer
- De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data (2018)
- Detailed analysis of HTT repeat elements in human blood using targeted amplification-free long-read sequencing (2018)
- Combination of short-read, long-read, and optical mapping assemblies reveals large-scale tandem repeat arrays with population genetic implications (2017)
- Clonal distribution of BCR-ABL1 mutations and splice isoforms by single-molecule long-read RNA sequencing (2015)
Senaste publikationer
- A novel quantitative targeted analysis of X-chromosome Inactivation (XCI) using Nanopore sequencing (2023)
- CRISPR-Cas9 induces large structural variants at on-target and off-target sites in vivo that segregate across generations (2022)
- SUPPLEMENTARY INFORMATION for CRISPR-Cas9 induces large structural variants at on-target and off-target sites in vivo (2021)
- Targeted Long-read Sequencing (2021)
- Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activity (2020)
Alla publikationer
Artiklar
- A novel quantitative targeted analysis of X-chromosome Inactivation (XCI) using Nanopore sequencing (2023)
- CRISPR-Cas9 induces large structural variants at on-target and off-target sites in vivo that segregate across generations (2022)
- Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activity (2020)
- Xdrop (2020)
- Xdrop (2020)
- Translating GWAS-identified loci for cardiac rhythm and rate using an in vivo image- and CRISPR/Cas9-based approach (2020)
- De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data (2018)
- Detailed analysis of HTT repeat elements in human blood using targeted amplification-free long-read sequencing (2018)
- Combination of short-read, long-read, and optical mapping assemblies reveals large-scale tandem repeat arrays with population genetic implications (2017)
- Clonal distribution of BCR-ABL1 mutations and splice isoforms by single-molecule long-read RNA sequencing (2015)
- CRISPR-Cas9 induces large structural variants at on-target and off-target sites in vivo
- Kita crispants for systematic image-based genetic screens of complex traits in zebrafish larvae