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Thread | Thread Starter | Forum | Replies | Last Post |
PacBio, SMART, assembly problem of de novo small genome | iuliachiciudean | Pacific Biosciences | 5 | 01-08-2019 09:08 PM |
BAC vector sequece masking for de novo assembly using PacBio C2 | Champi | Pacific Biosciences | 6 | 05-27-2013 02:59 AM |
De novo assembly of PacBio with short Illumina data | boetsie | Pacific Biosciences | 1 | 10-06-2012 01:35 PM |
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#1 |
Junior Member
Location: France Join Date: Jun 2019
Posts: 3
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Hello, I was given all the outputs of the result of a whole genome sequencing of a bacteria, and there is a lot of them and I don’t understand which one of these I should use to do a novo assembly:
I was thinking using SMRT link to do the analysis , but I don’t know which one of these I should use. Thanks in advance. |
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#2 |
Senior Member
Location: East Coast USA Join Date: Feb 2008
Posts: 7,091
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If you are planning to use SMRTlink then use the bax and bas files.
There are other options like flye (https://github.com/fenderglass/Flye ) and canu (https://github.com/marbl/canu) that may be better than SMRTlink and they can use the fastq files. |
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#3 |
Junior Member
Location: France Join Date: Jun 2019
Posts: 3
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Thank you for your answer
![]() I allready try canu but for somme resons it dosn't get installed... I will try to have a look at flye But for SMRT link I don't understand to what the bas and bax files correspond to (see image) ![]() |
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#4 |
Junior Member
Location: Bay Area, CA Join Date: Mar 2017
Posts: 1
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Import your metadata.xml file as "RSII Metadata (XML)" data type.
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Tags |
novo assemby, output, pacbio, smrt link |
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