This study quantifies the reasons for why some gene variants can be found as both germline and tumor specific (somatic) events https://t.co/6i5EsCKN3q
RT @WillMeyerson: >300K somatic variants in TCGA cancers are also listed as germline variants in gnomAD. Why this overlap? Now in BMC Bioin…
RT @WillMeyerson: >300K somatic variants in TCGA cancers are also listed as germline variants in gnomAD. Why this overlap? Now in BMC Bioin…
RT @WillMeyerson: >300K somatic variants in TCGA cancers are also listed as germline variants in gnomAD. Why this overlap? Now in BMC Bioin…
RT @WillMeyerson: >300K somatic variants in TCGA cancers are also listed as germline variants in gnomAD. Why this overlap? Now in BMC Bioin…
RT @WillMeyerson: >300K somatic variants in TCGA cancers are also listed as germline variants in gnomAD. Why this overlap? Now in BMC Bioin…
RT @WillMeyerson: >300K somatic variants in TCGA cancers are also listed as germline variants in gnomAD. Why this overlap? Now in BMC Bioin…
RT @WillMeyerson: >300K somatic variants in TCGA cancers are also listed as germline variants in gnomAD. Why this overlap? Now in BMC Bioin…
RT @WillMeyerson: >300K somatic variants in TCGA cancers are also listed as germline variants in gnomAD. Why this overlap? Now in BMC Bioin…
>300K somatic variants in TCGA cancers are also listed as germline variants in gnomAD. Why this overlap? Now in BMC Bioinformatics as my 1st 1st-author work. https://t.co/ZeGIE18yMf w/ John Leisman, @FNavarroBioInfo, @MarkGerstein https://t.co/5IEEVpaPa
RT @BMCBioinfo: Origins and characterization of variants shared between databases of somatic and germline human mutations https://t.co/1egg…
Origins and characterization of variants shared between databases of somatic and germline human mutations https://t.co/1egg9mfkvV #bioinformatics