Application of targeted nanopore sequencing for the screening and determination of structural variants in patients with Lynch syndrome
Lynch syndrome is a hereditary disease characterized by an increased risk of colorectal and other cancers. Germline variants in the mismatch repair (MMR) genes are responsible for this disease. Previously, we screened the MMR genes in colorectal cancer patients who fulfilled modified Amsterdam II cr...
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Published in: | Journal of human genetics Vol. 66; no. 11; pp. 1053 - 1060 |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
England
Nature Publishing Group
01-11-2021
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Subjects: | |
Online Access: | Get full text |
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