BIOM-12. ULTRA-DEEP WHOLE GENOME SEQUENCING UNCOVERS A HIGH PREVALENCE OF GLIOBLASTOMA-DERIVED CELL-FREE DNA IN PLASMA von Underhill, Hunter, Farrell, Andrew, Dean, Charlie, Harrison, Brion, Bronner, Mary, Colman, Howard, Jensen, Randy

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BIOM-53. LOW-PASS WHOLE GENOME SEQUENCING OF CEREBROSPINAL FLUID IDENTIFIES TUMOR AGNOSTIC TP53 ABERRATIONS IN LEPTOMENINGEAL METASTATIC DISEASE von Malani, Rachna, Zhang, Yingqi, Dean, Charlie, Boatz, Laura, Harrison, Brion, Wei, Mei, Akerley, Wallace, Bronner, Marry, Underhill, Hunter

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Abstract 212: True2 duplex sequencing reveals a diverse landscape of unique somatic mutations beyond the surgical margins of high- and low-grade diffuse gliomas von Underhill, Hunter, Karsy, Michael, Davidson, Christian, Hellwig, Sabine, Stevenson, Samuel, Vincenti, Sydney, Dean, Charlie, Harrison, Brion, Goold, Eric, Bronner, Mary, Colman, Howard, Jensen, Randy

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Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data von Chen, Guo-Bo, Lee, Sang Hong, Brion, Marie-Jo A, Montgomery, Grant W, Wray, Naomi R, Radford-Smith, Graham L, Visscher, Peter M

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Forensic validation of the SNPforID 52-plex assay von Musgrave-Brown, Esther, Ballard, David, Balogh, Kinga, Bender, Klaus, Berger, Burkhard, Bogus, Magdalena, Børsting, Claus, Brion, María, Fondevila, Manuel, Harrison, Cheryl, Oguzturun, Ceylan, Parson, Walther, Phillips, Chris, Proff, Carsten, Ramos-Luis, Eva, Sanchez, Juan J, Sánchez Diz, Paula, Sobrino Rey, Bea, Stradmann-Bellinghausen, Beate, Thacker, Catherine, Carracedo, Angel, Morling, Niels, Scheithauer, Richard, Schneider, Peter M, Syndercombe Court, Denise

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Population studies using single nucleotide polymorphisms—how important is detailed sample origin information? von Thacker, C., Harrison, C., Brion, M., Phillips, C., Sanchez-Diz, P., Ballard, D., Carracedo, A., Syndercombe Court, D.

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Post-translational modifications of cytoskeletal proteins von Anderton, B., Calvert, R., Gallo, J-M., Hanger, D., Harrison, L., Brion, J-P.

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