Live data from Hacker News

Viewing profile — gpurkins

gpurkins

HN member
Joined
Fri, Mar 30, 2012, 1:29 AM UTC
HN karma
10
Public activity
13 items

About gpurkins

No profile information was provided.

Recent public activity

  1. comment
    Comment #6779010

    "oh no I have so many amazing tools to choose from?", I use puppet at the moment. Any of them will make your deploy/config life great.

  2. comment
    Comment #6659587

    Nice! I had read something similar for a wood workshop here: http://woodgears.ca/dust/air_cleaner.html Seems to be quite effective. Also, if you're into woodworking, woodgears is p…

  3. comment
    Comment #5916580

    https://banyan.co/ collaboration for scientists on OSX

  4. comment
    Comment #5609875

    A good version exists here: http://www.planetmule.com/

  5. comment
    Comment #5379551

    http://prserve.com is quite good.

  6. comment
    Comment #5357489

    Sparkfun also has an exceptional write up on how to get into the microamp ballpark: http://www.sparkfun.com/tutorials/309 The article's try and see approach is very detailed and a …

  7. comment
    Comment #5069750

    Thin clients ride again. How much will Dell charge to run your instances?

  8. comment
    Comment #4691139

    Use an open format and learn to love the bomb? Districts probably aren't going to care, as they are looking for a cheaper way to stay current. I recognize the prices are not as goo…

  9. story
  10. comment
    Comment #3774409

    The point is to look at genomic variations across the entirety of the human genome, not so much to match genomic variation to phenotype. What you're saying makes sense, but I think…

  11. comment
    Comment #3774105

    http://en.wikipedia.org/wiki/1000_Genomes_Project Here's the project explanation, but the data itself is 1000 complete (hopefully!) genome sequences. The hope is to find the varian…

  12. comment
    Comment #3774094

    Depends, there are several sequencing technologies and they all have strengths/weaknesses. At my job, we use 454 sequencing from Roche and since it relies on PCR it has problems wi…

  13. comment
    Comment #3774086

    The real reason for a lot of this is personalized medicine, or rather more specific medicine. A gene translocation or even a SNP may be able to differentiate cancer types and chang…