12 - A Comprehensive Genomic Tool for Combined Interpretation and Reporting of Sequence Variants and Copy Number Changes Assessed by Different Platforms
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Published in | Cancer genetics Vol. 214-215; pp. 35 - 36 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Inc
01.08.2017
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Online Access | Get full text |
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ISSN: | 2210-7762 2210-7770 |
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DOI: | 10.1016/j.cancergen.2017.04.013 |