Results: 4

1.
Figure 4

Figure 4. From: Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples.

Benchmarking mutation detection methods. (a) Comparison of sensitivity as a function of tumor sequencing depth and mutation allele fraction for different mutation detection methods and configurations. (b) Comparison of somatic miscall error rate for true germline sites as a function of sequencing depth in the normal. (c) Comparison of somatic miscall error rate for true reference sites as a function of tumor sequencing depth. (d) Sensitivity as a function of specificity for mutations with an allele fraction of 0.1, tumor depth of 30x and normal depth of 30x between different methods and configurations. Black dotted lines indicate change in sensitivity and specificity between STD and HC configurations for a method. Grey solid lines are the MuTect results of virtual tumor approach from . (a–c) Error bars represent 95% CIs.

Kristian Cibulskis, et al. Nat Biotechnol. ;31(3):213-219.
2.
Figure 1

Figure 1. From: Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples.

Overview of somatic point mutation detection using MuTect.
MuTect takes as input tumor (T) and normal (N) next generation sequencing data and, after removing low quality reads (), determines if there is evidence for a variant beyond the expected random sequencing errors. Candidate variant sites are then passed through six filters to remove artifacts (). Next, a Panel of Normals is used to screen out remaining false positives caused by rare error modes only detectable in additional samples. Finally, the somatic or germline status of passing variants is determined using the matched normal.

Kristian Cibulskis, et al. Nat Biotechnol. ;31(3):213-219.
3.
Figure 3

Figure 3. From: Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples.

Specificity of variant detection and variant classification using virtual tumor approach. (a) Somatic miscall error rate for true reference sites as a function of tumor sequencing depth for the STD (red), HC (blue) and HC+PON (green) configurations of MuTect. Error bars represent 95% CIs. (b) Distribution of allele fraction for all miscalls as a function of tumor sequencing depth. (c) Fraction of events rejected by each filter; hashed regions indicate events rejected exclusively by each filter. (d) Somatic miscall error rate for true germline SNP sites by sequencing depth in the normal when the site is known to be variant in the population (blue) and novel (red). Error bars represent 95% CIs. (e,f) Mean power as a function of sequencing depth in the normal to have classified these events as germline or somatic at novel germline sites (e) and known germline variant sites (f).

Kristian Cibulskis, et al. Nat Biotechnol. ;31(3):213-219.
4.
Figure 2

Figure 2. From: Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples.

Sensitivity as a function of sequencing depth and allelic fraction.
(a) Sensitivity and specificity of MuTect for mutations with an allele fraction of 0.2, tumor depth of 30x and normal depth of 30x using various values of the LOD threshold (θT) (0.1 ≤ θT ≤ 100). Results using a model of independent sequencing errors with uniform Q35 base quality scores and accurate read placement (solid grey) are shown as well as results from the virtual tumor approach for the standard (STD, dashed green) and high-confidence (HC, solid green) configurations. A typical setting of θT = 6.3 is marked with black circles. (b) Sensitivity as a function of tumor sequencing depth and allele fraction (indicated by color) using θT = 6.3. The calculated sensitivity using a model of independent sequencing errors and accurate read placement with uniform Q35 base quality scores (solid lines) are shown as well as results from the virtual tumor approach (circles) and the downsampling of validated colorectal mutations (diamonds). Error bars represent 95% CIs.

Kristian Cibulskis, et al. Nat Biotechnol. ;31(3):213-219.

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