The authors of "Tumor sequencing is useful to refine the analysis…" (https://t.co/2O6IwIybfY) included RRIDs in their paper! RRIDs like this improve reproducibility in scientific research. #accelerateopenscience #STMpublishing
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RT @LiteratureFeed: Mutational Signatures: Tumor sequencing is useful to refine the analysis of germline variants in unexplained high-risk…
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Mutational Signatures: Tumor sequencing is useful to refine the analysis of germline variants in unexplained high-risk breast cancer families. https://t.co/b9UWCAK5kS https://t.co/VHt2EzacY1
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Tumor sequencing is useful to refine the analysis of germline variants in unexplained high-risk breast cancer families. https://t.co/dhY0sy8ex4