Closed aechchiki closed 5 years ago
Hi Amina,
I'm working on a new version of the tool that will do both assembly polishing and phasing, and my early results are very promising. But, to answer your question, you should start with the haploid sequence.
On Fri, Nov 16, 2018 at 5:51 AM Amina Echchiki notifications@github.com wrote:
Hi @benedictpaten https://github.com/benedictpaten
thanks for delivering this tool.
We would like to see its performance for haplotyping a genome which we generated through Canu https://github.com/marbl/canu. The organism is diploid but highly heterozygous, haploid size aprox. 500Mbp. We also have the raw files (PacBio RSII).
For your pipeline to be more effective, shall I use as reference the diploid (Canu) or the haploid sequence (for now I have tested Haplomerger2 https://github.com/mapleforest/HaploMerger2 and PurgeHaplotigs https://bitbucket.org/mroachawri/purge_haplotigs post-Canu)? So I am just wondering which fasta reference to feed to your program.
Thanks, Amina
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thanks for your answer! will use the haploid sequence then!
looking forward for your tool update, Amina
Hi @benedictpaten
thanks for delivering this tool.
We would like to see its performance for haplotyping a genome which we generated through Canu. The organism is diploid but highly heterozygous, haploid size aprox. 500Mbp. We also have the raw files (PacBio RSII).
For your pipeline to be more effective, shall I use as reference the diploid (Canu) or the haploid sequence (for now I have tested Haplomerger2 and PurgeHaplotigs post-Canu)? So I am just wondering which fasta reference to feed to your program.
Thanks, Amina