Question: Macrogen Vs Complete Genomics
2
gravatar for Biomed
7.8 years ago by
Biomed4.5k
Bethesda, MD, USA
Biomed4.5k wrote:

We are pondering to outsource couple (around 20) whole human genome sequencing (mostly Mendelian disease/gene hunting in nuclear families) projects. Out two top candidates now are Macrogen (Illumina partner) and Complete Genomics.

My question is mainly to those who have worked with either of these companies and even better with both of them. What would your recommendations be? Are their data quality, services comparable? Also some other important things are turn around time and easy file formats, annotations so we can effectively pick up and continue the analysis down stream. Any comments regarding what type of strengths and weaknesses they have are much appreciated, I assume detection of snps would not change too much between two approaches but what about other things (i.e being able to detect larger indels, balanced translocations etc)? Do you have any specific recommendations that might help us in our decision?

genome sequencing • 2.0k views
ADD COMMENTlink modified 7.6 years ago by lh331k • written 7.8 years ago by Biomed4.5k
5
gravatar for lh3
7.8 years ago by
lh331k
United States
lh331k wrote:

I am not able to comment on macrogen. As to Complete Genomics (CG), you should ask yourself about how many analyses you want to do by yourself. CG has a very sophisticated pipeline. If you want to leave your project to them, CG will be a decent choice. However, if you want to get their data and analyze by yourself, you should watch out. While you have a variety of choices of software for analyzing Illumina data, the CG software package is pretty much the only one that is able to process the CG reads and alignments. When you have troubles with their results, you can hardly get help elsewhere except CG (their support seems good; I have sent them a couple of requests and all got replies in hours).

ADD COMMENTlink written 7.8 years ago by lh331k

Would this comment apply to the pipeline which would create a variant/genotype call output like mpileup output?

ADD REPLYlink written 7.8 years ago by Biomed4.5k

The RTG Investigator package from www.realtimegenomics.com includes support for mapping (to SAM) and variant calling (to VCF) from Complete Genomics read data.

ADD REPLYlink written 7.8 years ago by Len Trigg1.2k
1
gravatar for Larry_Parnell
7.8 years ago by
Larry_Parnell16k
Boston, MA USA
Larry_Parnell16k wrote:

Complete Genomics has made available data from 69 individuals. I picked up a copy on thumb drive at a recent conference but have yet to use those data. I know it is available from the web site. You could grab those data and take a look for yourself regarding data quality.

Check out the Assemblathon and ask those folks these same questions. While not directly related to your question, the Assemblathon was a test of different assembly algorithms but those involved surely would be able to comment on data quality.

ADD COMMENTlink written 7.8 years ago by Larry_Parnell16k

I also wonder what Macrogen offers in terms of processed data. At least from CG's marketing, they offer pretty good variant calling and filtering.

ADD REPLYlink written 7.8 years ago by brentp22k

Assamblathon kindly declined to answer this question and refereed me to seqanswers eventhough I told them I had originally asked the question here and got refreed to their list:)

ADD REPLYlink written 7.8 years ago by Biomed4.5k

OK, so they do not wish to take sides and are being diplomatic. That's fine. Did seqanswers give anything useful?

ADD REPLYlink written 7.8 years ago by Larry_Parnell16k
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