Author

Aleksandra Krstic

Karolinska University Hospital

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

Biology Disciplines

Click to filter author papers

Genetics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 2 Research Focus:variant calling· 2 Assay:bulk RNA-seq· 1 Organism:human· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Charlotte GustafssoniD· 2 shared Julia HauensteiniD· 2 shared Nicolai Sebastian FrengeniD· 2 shared Robert MånssoniD· 2 shared Ann Wallblom· 1 shared Anna LindstrandiD· 1 shared Charlotte GraniD· 1 shared Fanny Taborsak-LinesiD· 1 shared

Activity by Year

2022-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersMolecular Biology

Charlotte GustafssonORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

T-RHEX-RNAseq - A tagmentation-based, rRNA blocked, random hexamer primed RNAseq method for generating stranded RNAseq libraries directly from very low numbers of lysed cells.

Charlotte Gustafsson, Julia Hauenstein, Nicolai Sebastian Frengen, Aleksandra Krstic, Sidinh Luc, Robert Månsson

The paper introduces T-RHEX-RNAseq, a method for generating stranded RNAseq libraries from very low numbers of lysed cells without RNA purification steps.

bioRxiv · Oct 20, 2022 · PreprintMolecular Biology

Linked-read whole-genome sequencing resolves common and private structural variants in multiple myeloma

Lucía Peña‐Pérez, Nicolai Sebastian Frengen, Julia Hauenstein, Charlotte Gran, Charlotte Gustafsson, Jesper Eisfeldt, Marcin Kierczak, Fanny Taborsak-Lines, Remi‐André Olsen, Ann Wallblom, Aleksandra Krstic, Philip Ewels, Anna Lindstrand, Robert Månsson

This study uses linked-read whole-genome sequencing to detect structural variants and copy number variations in multiple myeloma, identifying both common and private variants that affect gene regulation and molecular classification.

Blood Advances · Jun 8, 2022Peer-reviewedGenetics