Genome Analysis Toolkit

Variant Discovery in High-Throughput Sequencing Data

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Developed in the Data Sciences Platform at the Broad Institute, the toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. Its powerful processing engine and high-performance computing features make it capable of taking on projects of any size. Learn more

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Number of Ns at the pileup

Category Variant Annotations

Overview

Apply a read-based annotation that reports the number of Ns seen at a given site. This is intended for use on consensus called data.

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GATK version 4.1.9.0-SNAPSHOT built at Mon, 19 Oct 2020 11:41:12 -0400.

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