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