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Summary
DescriptionHeterozygous SNV call, from aligned NGS reads.png
Image which visually depicts how aligned NGS read data against a reference can be used to call SNVs. In this picture a possible heterozygous variant is shown, with some reads containing the nucleotide G and others A, against the reference allele A.
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Benno89 at English Wikipedia, the copyright holder of this work, hereby publishes it under the following licenses:
Permission is granted to copy, distribute and/or modify this document under the terms of the GNU Free Documentation License, Version 1.2 or any later version published by the Free Software Foundation; with no Invariant Sections, no Front-Cover Texts, and no Back-Cover Texts. A copy of the license is included in the section entitled GNU Free Documentation License.http://www.gnu.org/copyleft/fdl.htmlGFDLGNU Free Documentation Licensetruetrue
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