Originally posted by frozenlyse
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Originally posted by rskr View PostYep it was more important when you have 36mers to know how bad the alignments with them are. Now that we have 100mers, we can be a little more confident in our alignments.
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Phillip
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Originally posted by pmiguel View PostWell, don't be coy. What benchmarking protocol would satisfy you? Please be specific.
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Phillip
BWA, comes with a test suite, that will generate randomized reads, and evaluate them.
Pretty easy, only reason not to do it is you know it isn't good.
wgsim does do some error modeling and biological zygosity, but it doesn't do a very sophisticated job of the error modeling such as quality and error decreasing at the ends of reads, so it is still somewhat optimistic. Also the scoring is a little odd it doesn't measure the exact SNPs, and indels, but only if the reads were in the right place +-5bp, and if a read maps wrong multiple times that counts against the error multiple. That could be improved, but it will give a pretty good idea of what the accuracy really is.
The best thing about bench marking? Its cheap!
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Innovations in next-generation sequencing technologies and techniques are driving more precise and comprehensive exploration of complex biological systems. Current advancements include improved accessibility for long-read sequencing and significant progress in single-cell and 3D genomics. This article explores some of the most impactful developments in the field over the past year.
Long-Read Sequencing
Long-read sequencing has seen remarkable advancements,...-
Channel: Articles
12-02-2024, 01:49 PM -
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