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X-WR-CALNAME;VALUE=TEXT:Analyzing NGS Data: Standard data processing and workflow analysis on high powered computing environment
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SUMMARY:Analyzing NGS Data: Standard data processing and workflow analysis on high powered computing environment
DESCRIPTION:<p>	The NGS technologies have the potential to dramatically accelerate biomedical research by enabling<br>comprehensive analysis of genomes and transcriptomes to become inexpensive, routine, and<br>widespread tools. This workshop will focus on methods for base‐calling and variant‐calling, for aligning<br>reads to reference sequences (e.g. genomes), and for de novo assembly of short reads into longer<br>sequences. The following tools will be covered on Orchestra, a shared research cluster; quality reports<br>of FASTQ files, trimming and filtering of reads, alignment and coverage objects such as SAM/BAM files<br>using bowtie/bwa, calling SNPs with Samtools, and De novo Assembly using Velvet.</p><p>	Register <a data-url="https://libcal.library.harvard.edu/event/4665149" href="https://libcal.library.harvard.edu/event/4665149" title="">here</a></p>
LOCATION:Countway Floor L2: 025
STATUS:CONFIRMED
DTSTART:20181128T150000Z
DTEND:20181128T180000Z
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