Скачать или смотреть Short Read Mapping: The foundation of next generation sequencing analysis

Data generated from high throughput DNA sequencing technology can be used for many diverse applications, such as variant calling or enrichment detection from a pool of sequenced DNA. A key part of many pipelines where a reference genome exists (e.g. human or model organisms) is mapping the short sequences back to the reference genome.

In this webinar, we walk through the process of mapping and visualizing reads from diverse datasets including ChIP-seq and ATAC-seq, which can provide insight into the transcriptional regulation of genes. In order to cover the material we will be proceeding at a fast pace. Following along with the presentation may be possible for experienced users. To enable followup learning and self-paced exploration after the webinar, the speaker will deposit functional scripts and example datasets on the Cedar compute cluster.

To view / download the slides from this presentation, visit:
https://westgrid.github.io/trainingMa...

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