10.1371/journal.pone.0184608.g001
Riku Walve
Riku
Walve
Leena Salmela
Leena
Salmela
Veli Mäkinen
Veli
Mäkinen
Recall (a) and precision (b) scores for simulated insertions.
Public Library of Science
2017
insertion genotyping
genome assembly
insertion genotyping tools
reference genome
insertion sequence
insertion variants
method
DNA
gap
genotyping insertion variants
genome assembly projects
2017-09-08 18:15:43
Figure
https://plos.figshare.com/articles/figure/Recall_a_and_precision_b_scores_for_simulated_insertions_/5392684
<p>Filtering is tested with three simulated read sets with different insert size distributions. As the results for our proposed filtering scheme differ based on the insert size distributions, we have separated and labeled them with the corresponding mean insert sizes, <i>μ</i> = 150, 1500, 3000. The other two are averaged over all the read sets. The dashed lines for Filter use only reads that are filtered in and the solid lines add all unmapped reads to the filtered read set if the coverage of the filtered reads is below the coverage threshold (here 25). The precision of using all unmapped reads is almost zero and is thus not visible in the graph.</p>