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Chunk #34 — 3 RESULTS — 3.3 Evaluation of models on a deeply sequenced breast cancer genome with ground truth SNVs

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SNVMix: predicting single nucleotide variants from next-generation sequencing of tumors.
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of Q1 base quality thresholds.) This suggests that previously reported base quality thresholds may be too stringent. Furthermore, when used with stringent mapping quality thresholds, the SNVMix2 model can effectively use the base qualities by probabilistic weighting to confer higher accuracy. These results indicate that treating mapping and base qualities separately as opposed to taking a minimum over the two (as in Maq) has advantages.