Bjorn Stade

Kiel, SH 24118, Germany

Last Updated: 09/26/2026

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Found 8 publications

New technologies for DNA analysis--a review of the READNA Project.

New technologies for DNA analysis--a review of the READNA Project.

Journal: New biotechnology
Published: August 11, 2015

Genomics and drug profiling of fatal TCF3-HLF-positive acute lymphoblastic leukemia identifies recurrent mutation patterns and therapeutic options.

Genomics and drug profiling of fatal TCF3-HLF-positive acute lymphoblastic leukemia identifies recurrent mutation patterns and therapeutic options.

Journal: Nature genetics
Published: December 02, 2014

Early-onset Crohn's disease and autoimmunity associated with a variant in CTLA-4.

Early-onset Crohn's disease and autoimmunity associated with a variant in CTLA-4.

Journal: Gut
Published: September 30, 2014

GrabBlur--a framework to facilitate the secure exchange of whole-exome and -genome SNV data using VCF files.

GrabBlur--a framework to facilitate the secure exchange of whole-exome and -genome SNV data using VCF files.

Journal: BMC genomics
Published: July 25, 2014

Whole genome and exome sequencing of monozygotic twins discordant for Crohn's disease.

Whole genome and exome sequencing of monozygotic twins discordant for Crohn's disease.

Journal: BMC genomics
Published: April 25, 2014

Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies.

Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies.

Journal: Gastroenterology
Published: December 07, 2012

From next-generation sequencing alignments to accurate comparison and validation of single-nucleotide variants: the pibase software.

From next-generation sequencing alignments to accurate comparison and validation of single-nucleotide variants: the pibase software.

Journal: Nucleic acids research
Published: September 12, 2012

Improving mapping and SNP-calling performance in multiplexed targeted next-generation sequencing.

Improving mapping and SNP-calling performance in multiplexed targeted next-generation sequencing.

Journal: BMC genomics
Published: November 10, 2011
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Last Updated: 09/26/2026