Forum: ngs vs microarray
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gravatar for au.rinki.bio
16 months ago by
au.rinki.bio10
University of Allahabad, India
au.rinki.bio10 wrote:

With all the advancements that NGS has made, why is anyone still using microarrays?

ADD COMMENTlink modified 16 months ago by lakhujanivijay4.5k • written 16 months ago by au.rinki.bio10
3

It should be pointed out that NGS has pitfalls that have prevented its enrollment in clinical settings; whereas, microarray technology and its analysis methods are mature and have been used in the clinic for decades. Sanger sequencing, array CGH, FISH, PCR, etc., are still the gold standards in clinical genetics - NGS is a poor and 'cheap' substitute to these

So, despite the fact that large companies have pushed NGS onto us, inherent errors in this technology have not been talked about and have been somewhat buried in technology white papers.

ADD REPLYlink modified 16 months ago • written 16 months ago by Kevin Blighe51k
1

A timely blog post for your question:

Sequencing or Array Testing for Genetic Diseases?

ADD REPLYlink written 16 months ago by h.mon28k

I moved this to a forum post.

ADD REPLYlink written 16 months ago by Jean-Karim Heriche21k
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gravatar for Jean-Karim Heriche
16 months ago by
EMBL Heidelberg, Germany
Jean-Karim Heriche21k wrote:

There are probably many reasons. One may be the weight of inertia. If you know a technology and it works for you, there's little reason to switch to something else. For some applications, microarrays may be cheaper than NGS, especially if you factor in the cost of analysis because data handling and analysis is also more complex for NGS than for microarray. In addition rapid changes in technology and pipelines makes NGS feel like a less mature approach than microarray.

ADD COMMENTlink written 16 months ago by Jean-Karim Heriche21k
5
gravatar for lakhujanivijay
16 months ago by
lakhujanivijay4.5k
India
lakhujanivijay4.5k wrote:

CGH arrays are employed to detect chromosomal aberrations. Focussing on human genetic disorders, most of the major hospitals and diagnostic centres in the US have happily adapted microarrays. Thousands of samples are analysed on daily basis for a number of patients. Microarrays are allowing analysis , QC and sample preparation in large batches with cheaper costs.

Secondly, as mentioned above, researchers are comfortable with the analysis. Companies like Illumina and Agilent are providing free-of-cost workflow based software for microarray analysis which requires minimum knowledge of computers. On the other hand, most of the NGS based tools are open source and requires basic understanding of Linux. The transition is happening gradually but it will take time because the technology is different, the raw data is different and the down-stream analysis is also very much different.

ADD COMMENTlink modified 6 months ago • written 16 months ago by lakhujanivijay4.5k
4
gravatar for dariober
16 months ago by
dariober10k
WCIP | Glasgow | UK
dariober10k wrote:

I don't have much experience with genotyping arrays but I think these are an example where arrays are still superior to NGS. If you want to profile a sample at known SNPs genomewide, then it's going to be difficult for NGS to beat arrays in terms of cost, amount of data to process and accuracy. I think with arrays you can genotype tens or hundreds of samples for the price of a whole genome sequence and you need to process gigabytes of data instead of terabytes.

ADD COMMENTlink written 16 months ago by dariober10k
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