article Open AccessTop 10% cited
Sequenza: allele-specific copy number and mutation profiles from tumor sequencing data
Annals of Oncology · 2014 · Vol. 26(1) · pp. 64–70
Francesco Favero(Technical University of Denmark)Trupti Joshi(Technical University of Denmark)Andrea Marion Marquard(Technical University of Denmark)Nicolai J. Birkbak(Technical University of Denmark)Marcin Krzystanek(Technical University of Denmark)Qingshun Quinn Li(Xiamen University)Zoltán Szállási(Harvard–MIT Division of Health Sciences and Technology)Aron C. Eklund✉(Technical University of Denmark)
Cancer Genomics and DiagnosticsGenetic factors in colorectal cancerLung Cancer Treatments and MutationsMedicineAlleleGeneticsMutationDNA sequencingComputational biologyGeneBiology
MeSH terms
AlgorithmsAllelesBase SequenceHumansMutationNeoplasmsSoftwareSequence Analysis, DNAGene DosagePolymorphism, Single NucleotideDNA Copy Number VariationsHigh-Throughput Nucleotide SequencingExome
Funding
- Breast Cancer Research Foundation
- European Commission
- Danmarks Frie Forskningsfond
- National Cancer Institute
Citations
898
FWCI
7.55
field-weighted impact
References
28
Percentile
98%
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References
The Sequence Alignment/Map format and SAMtools
Bioinformatics · 2009 · 66,208 citations
Intratumor Heterogeneity and Branched Evolution Revealed by Multiregion Sequencing
New England Journal of Medicine · 2012 · 7,706 citations
VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing
Genome Research · 2012 · 5,265 citations
Absolute quantification of somatic DNA alterations in human cancer
Nature Biotechnology · 2012 · 2,193 citations
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