Related references
Note: Only part of the references are listed.Strategy for Robust Detection of Insertions, Deletions, and Point Mutations in CEBPA, a GC-Rich Content Gene, Using 454 Next-Generation Deep-Sequencing Technology
Vera Grossmann et al.
JOURNAL OF MOLECULAR DIAGNOSTICS (2011)
Targeted next-generation sequencing detects point mutations, insertions, deletions and balanced chromosomal rearrangements as well as identifies novel leukemia-specific fusion genes in a single procedure
V. Grossmann et al.
LEUKEMIA (2011)
SLOPE: a quick and accurate method for locating non-SNP structural variation from targeted next-generation sequence data
Haley J. Abel et al.
BIOINFORMATICS (2010)
Fast and accurate long-read alignment with Burrows-Wheeler transform
Heng Li et al.
BIOINFORMATICS (2010)
Analysing 454 amplicon resequencing experiments using the modular and database oriented Variant Identification Pipeline
Joachim M. De Schrijver et al.
BMC BIOINFORMATICS (2010)
Next-Generation Sequencing Technology Reveals a Characteristic Pattern of Molecular Mutations in 72.8% of Chronic Myelomonocytic Leukemia by Detecting Frequent Alterations in TET2, CBL, RAS, and RUNX1
Alexander Kohlmann et al.
JOURNAL OF CLINICAL ONCOLOGY (2010)
ShortRead: a bioconductor package for input, quality assessment and exploration of high-throughput sequence data
Martin Morgan et al.
BIOINFORMATICS (2009)
The Sequence Alignment/Map format and SAMtools
Heng Li et al.
BIOINFORMATICS (2009)
Share Paper
