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Comprehensive detection of recurring genomic abnormalities: a targeted sequencing approach for multi...

Comprehensive detection of recurring genomic abnormalities: a targeted sequencing approach for multi...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_swepub_primary_oai_swepub_ki_se_474966

Comprehensive detection of recurring genomic abnormalities: a targeted sequencing approach for multiple myeloma

About this item

Full title

Comprehensive detection of recurring genomic abnormalities: a targeted sequencing approach for multiple myeloma

Publisher

London: Nature Publishing Group UK

Journal title

Blood cancer journal (New York), 2019-12, Vol.9 (12), p.101-101, Article 101

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Recent genomic research efforts in multiple myeloma have revealed clinically relevant molecular subgroups beyond conventional cytogenetic classifications. Implementing these advances in clinical trial design and in routine patient care requires a new generation of molecular diagnostic tools. Here, we present a custom capture next-generation sequenc...

Alternative Titles

Full title

Comprehensive detection of recurring genomic abnormalities: a targeted sequencing approach for multiple myeloma

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_swepub_primary_oai_swepub_ki_se_474966

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_swepub_primary_oai_swepub_ki_se_474966

Other Identifiers

ISSN

2044-5385

E-ISSN

2044-5385

DOI

10.1038/s41408-019-0264-y

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