Susana Häggqvist

Clonal distribution of BCR-ABL1 mutations and splice isoforms by single-molecule long-read RNA sequencing

Cavelier, Lucia; Ameur, Adam; Häggqvist, Susana; Höijer, Ida et al.

Part of BMC Cancer, 2015

• DOI for Clonal distribution of BCR-ABL1 mutations and splice isoforms by single-molecule long-read RNA sequencing
• Download full text (pdf) of Clonal distribution of BCR-ABL1 mutations and splice isoforms by single-molecule long-read RNA sequencing

Comprehensive profiling of the vaginal microbiome in HIV positive women using massive parallel semiconductor sequencing

Ameur, Adam; Meiring, Tracy L.; Bunikis, Ignas; Häggqvist, Susana et al.

Part of Scientific Reports, p. 4398, 2014

• DOI for Comprehensive profiling of the vaginal microbiome in HIV positive women using massive parallel semiconductor sequencing
• Download full text (pdf) of Comprehensive profiling of the vaginal microbiome in HIV positive women using massive parallel semiconductor sequencing

Targeted RNA Sequencing Assay Efficiently Identifies Cryptic KMT2A (MLL)-Fusions in Acute Leukemia Patients

Sevov, Marie; Bunikis, Ignas; Häggqvist, Susana; Höglund, Martin et al.

Part of Blood, 2014

Whole-genome sequencing with AVITI and NovaSeq X Plus reveals comparable performance with contextual biases

Höjer, Pontus; Alneberg, Johannes; Lundin, Pär; Martin, Tom et al.

Part of NAR Genomics and Bioinformatics, 2026

• DOI for Whole-genome sequencing with AVITI and NovaSeq X Plus reveals comparable performance with contextual biases
• Download full text (pdf) of Whole-genome sequencing with AVITI and NovaSeq X Plus reveals comparable performance with contextual biases

Long-read whole-genome analysis of human single cells

Hård, Joanna; Mold, Jeff E; Eisfeldt, Jesper; Tellgren-Roth, Christian et al.

Part of Nature Communications, 2023

• DOI for Long-read whole-genome analysis of human single cells
• Download full text (pdf) of Long-read whole-genome analysis of human single cells

Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH

Lysenkova Wiklander, Mariya; Övernäs, Elin; Lagensjö, Johanna; Raine, Amanda et al.

Part of BMC Research Notes, 2023

• DOI for Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH
• Download full text (pdf) of Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH

Novel cancer gene discovery using a forward genetic screen in RCAS-PDGFB-driven gliomas

Weishaupt, Holger; Čančer, Matko; Rosén, Gabriela; Holmberg, Karl O. et al.

Part of Neuro-Oncology, p. 97-107, 2023

• DOI for Novel cancer gene discovery using a forward genetic screen in RCAS-PDGFB-driven gliomas
• Download full text (pdf) of Novel cancer gene discovery using a forward genetic screen in RCAS-PDGFB-driven gliomas

Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activity

Höijer, Ida; Johansson, Josefin; Gudmundsson, Sanna; Chin, Chen-Shan et al.

Part of Genome Biology, 2020

• DOI for Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activity
• Download full text (pdf) of Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activity

Whole-genome sequencing with AVITI and NovaSeq X Plus reveals comparable performance with contextual biases

Höjer, Pontus; Alneberg, Johannes; Lundin, Pär; Martin, Tom et al.

Part of NAR Genomics and Bioinformatics, 2026

• DOI for Whole-genome sequencing with AVITI and NovaSeq X Plus reveals comparable performance with contextual biases
• Download full text (pdf) of Whole-genome sequencing with AVITI and NovaSeq X Plus reveals comparable performance with contextual biases

Long-read whole-genome analysis of human single cells

Hård, Joanna; Mold, Jeff E; Eisfeldt, Jesper; Tellgren-Roth, Christian et al.

Part of Nature Communications, 2023

• DOI for Long-read whole-genome analysis of human single cells
• Download full text (pdf) of Long-read whole-genome analysis of human single cells

Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH

Lysenkova Wiklander, Mariya; Övernäs, Elin; Lagensjö, Johanna; Raine, Amanda et al.

Part of BMC Research Notes, 2023

• DOI for Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH
• Download full text (pdf) of Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH

Novel cancer gene discovery using a forward genetic screen in RCAS-PDGFB-driven gliomas

Weishaupt, Holger; Čančer, Matko; Rosén, Gabriela; Holmberg, Karl O. et al.

Part of Neuro-Oncology, p. 97-107, 2023

• DOI for Novel cancer gene discovery using a forward genetic screen in RCAS-PDGFB-driven gliomas
• Download full text (pdf) of Novel cancer gene discovery using a forward genetic screen in RCAS-PDGFB-driven gliomas

Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activity

Höijer, Ida; Johansson, Josefin; Gudmundsson, Sanna; Chin, Chen-Shan et al.

Part of Genome Biology, 2020

• DOI for Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activity
• Download full text (pdf) of Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activity

De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data

Ameur, Adam; Che, Huiwen; Martin, Marcel; Bunikis, Ignas et al.

Part of Genes, 2018

• DOI for De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data
• Download full text (pdf) of De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data

Clonal distribution of BCR-ABL1 mutations and splice isoforms by single-molecule long-read RNA sequencing

Cavelier, Lucia; Ameur, Adam; Häggqvist, Susana; Höijer, Ida et al.

Part of BMC Cancer, 2015

• DOI for Clonal distribution of BCR-ABL1 mutations and splice isoforms by single-molecule long-read RNA sequencing
• Download full text (pdf) of Clonal distribution of BCR-ABL1 mutations and splice isoforms by single-molecule long-read RNA sequencing

Comprehensive profiling of the vaginal microbiome in HIV positive women using massive parallel semiconductor sequencing

Ameur, Adam; Meiring, Tracy L.; Bunikis, Ignas; Häggqvist, Susana et al.

Part of Scientific Reports, p. 4398, 2014

• DOI for Comprehensive profiling of the vaginal microbiome in HIV positive women using massive parallel semiconductor sequencing
• Download full text (pdf) of Comprehensive profiling of the vaginal microbiome in HIV positive women using massive parallel semiconductor sequencing

Targeted RNA Sequencing Assay Efficiently Identifies Cryptic KMT2A (MLL)-Fusions in Acute Leukemia Patients

Sevov, Marie; Bunikis, Ignas; Häggqvist, Susana; Höglund, Martin et al.

Part of Blood, 2014