Overview of methods for variant calling from next-generation sequence data
[13.07.07] albertsen mewe13 metagenomics
Bioinformatics Consulting Operation at the Dana-Farber Cancer Institute
The IMPACT of INDEL realignment: Detecting insertions and deletions longer than 30 base pairs with ABRA
Determine new application spaces in the sequencing platform using visions systems
Preparation of RNA and QC for Expression Profiling John Kenny Centre for Genomic Research, University of Liverpool.
PHYTOPHTHORA GENOME SEQUENCING: A case study