Exact(2)
Furthermore, Mendelian disease variants and recurrent cancer somatic mutations share very similar distribution across types of functional effects.
Furthermore, Mendelian disease variants and recurrent cancer somatic mutations share very similar distributions across types of functional impacts, suggesting the discovery of Mendelian disease variants might be broad enough to cover major pathways.
Similar(6)
However, using the rearrangement barcodes, even Patient 10, a germline BRCA1 mutation carrier, shared very few rearrangements between BC1 and BC2 and a different clonal origin could be determined (Additional files 3 and 4).
Share very generously.
First, they should initially share very similar mtDNA.
The ancestral clones contained Pik3ca/Kdm6a mutations and may reflect the field-disease mutations shared among later tumors.
The phenotypes in families with INF2 mutations shared certain features.
We also asked if individuals with shared mutations and shared HLA alleles may also share TCR sequences.
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