Header Leaderboard Ad
Collapse
23andMe cuts cost to $399! UPDATED...cut to $99
Collapse
Announcement
Collapse
No announcement yet.
X
-
Razib Khan will store them for you: http://blogs.discovermagazine.com/gn...lic-genotypes/
-
Originally posted by Michael.James.Clark View PostI need to go into it more in-depth, but we can choose to share our data with each other through the 23andme.com site, right? I think I just need to switch it to public sharing with other users on the site.
Leave a comment:
-
I need to go into it more in-depth, but we can choose to share our data with each other through the 23andme.com site, right? I think I just need to switch it to public sharing with other users on the site.
Leave a comment:
-
-
How many people here went for this deal? We should do something fun with the data!
I downloaded my data and stuck it here: https://github.com/dbolser/genotyping_23andme
I put an idea for a wiki based 'genome game' here:
http://gmod.org/wiki/GSoC#IDEA_10:_T...g_better_crops
http://gmod.org/wiki/GSoC/IDEA_10
Could be fun! ;-)
Leave a comment:
-
Best $200 I every spent getting both my results and my mothers results. When I first got my results I never put much stock in the 5cm segments thinking that they were to small to be of any great consequence or to small to take any stock in the results. When I compared my mothers results at 5cm to my list at 5cm, removing the common countries gave me the list of these remaining countries from my list. These being a fairly good probability of coming from my fathers side.
Those countries were:
Palestinian
Greece
Albania
Syria
Morocco
Four others were:
Mexico
Bolivia
Belgium
Phillippines
The first group has both a geographical significance along with a historical connection.
The second group of Mexico, Bolivia and the Phillippines are most likely coming from my great great grandmother on my fathers side native to Mexico. The Belgium segment could be a wandering relative or an anomaly.
This first group makes me think of some cohort connection in the Roman army or someone coming up from Morocco into Iberia then to the British Isles. This certainly reinforces some of best case guess on my older origins.
Leave a comment:
-
Originally posted by westerman View PostIt is tempting. It is so hard to buy presents for my parents, sisters and brother. I bet this is one present that they haven't purchased for themselves!
Leave a comment:
-
Version 2 vs Version 3 chip set snps
Customers can expect to have the following approximate numbers of SNPs for their genotyping platform:
V2 only: 576,000 SNPs
V3 only: 967,000 SNPs
V2 + V3 (upgraded): 996,000 SNPs
http://spittoon.23andme.com/2011/01/...hat-to-expect/
We have new information pertaining to your previous inquiry. Our v3 platform includes 3066 SNPs on the Y chromosome and 2736 mitochondiral [sic] SNPs. Our v2 platform included 1752 SNPs on the Y chromosome and 1998 mitochondiral [sic] SNPs. The complete list is not yet available.
Best Regards,
The 23andMe Team
Leave a comment:
-
Originally posted by Joann View PostThat would be such a cool gift. Archive everybody's sequences and update the family tree every other year or so around the holidays.
Last year as a holiday gift I had my mother tested by 23andme. Since my father is no longer alive to sample, I am able to compare my results to my mothers results to see what snp's are coming from my father's DNA. I was able to confirm that the 4% Asian in my DNA score comes from my fathers side of the family. This confirmed my paper genealogy to my 23andme results and my native south american ancestor on my fathers side. This is one way this testing can be used. Diekenes Blog spot on population analysis is also another interesting aspect of this testing. Link below:
http://dodecad.blogspot.com/
Leave a comment:
-
Originally posted by dp05yk View PostI've been looking into 23andMe and I'm confused as to what they're actually offering. As a computer science student I'm not 100% on all the biology yet and it seems absurd that they're actually (re)sequencing your entire genome for $400. Is the state of sequencing technology such that $400 is a fair price, or is it not exactly what I'm thinking it is?
http://www.familytreedna.com/glossary.html
Leave a comment:
-
Originally posted by ECO View PostThey aren't resequencing...you basically get the results of a 500k SNP genotyping chip, but their value is the annotation and continued research into variants and health implications.
They actually just cut the price to $99...but you have to subscribe to a $5/month.
I appreciate their desire to reduce the entry costs, but I don't really like the subscription model, will be interesting to see how it pans out.
Looks like I'll be genotyping my whole family soon.Anyone know if you can download your entire dataset with the new pricing model?
https://www.23andme.com/help/
Leave a comment:
-
With this new pricing a new version 3 chip is being used for testing. The Version 2 chip had about 500k snp's. The new Version 3 has 1 Million snp's on the chip approximately. Some of these new snps are geared to medical identification. This new pricing includes both the ancestry as well as medical editions for the consumer. There are other testing alternatives as well in the market place. There is more information on this type of testing at the the following link:
http://isogg.org/wiki/23andMe_project
Leave a comment:
-
That would be such a cool gift. Archive everybody's sequences and update the family tree every other year or so around the holidays.
Leave a comment:
-
Originally posted by ECO View Post
They actually just cut the price to $99...but you have to subscribe to a $5/month.
I appreciate their desire to reduce the entry costs, but I don't really like the subscription model, will be interesting to see how it pans out.
Looks like I'll be genotyping my whole family soon.
Leave a comment:
-
thats cool Eco!
I would assume the data should be downloadable, but never tried first hand..
Leave a comment:
Latest Articles
Collapse
-
by seqadmin
Amplicon sequencing is a targeted approach that allows researchers to investigate specific regions of the genome. This technique is routinely used in applications such as variant identification, clinical research, and infectious disease surveillance. The amplicon sequencing process begins by designing primers that flank the regions of interest. The DNA sequences are then amplified through PCR (typically multiplex PCR) to produce amplicons complementary to the targets. RNA targets...-
Channel: Articles
03-21-2023, 01:49 PM -
-
by seqadmin
Targeted sequencing is an effective way to sequence and analyze specific genomic regions of interest. This method enables researchers to focus their efforts on their desired targets, as opposed to other methods like whole genome sequencing that involve the sequencing of total DNA. Utilizing targeted sequencing is an attractive option for many researchers because it is often faster, more cost-effective, and only generates applicable data. While there are many approaches...-
Channel: Articles
03-10-2023, 05:31 AM -
ad_right_rmr
Collapse
News
Collapse
Topics | Statistics | Last Post | ||
---|---|---|---|---|
Started by seqadmin, 03-24-2023, 02:45 PM
|
0 responses
10 views
0 likes
|
Last Post
by seqadmin
03-24-2023, 02:45 PM
|
||
Started by seqadmin, 03-22-2023, 12:26 PM
|
0 responses
13 views
0 likes
|
Last Post
by seqadmin
03-22-2023, 12:26 PM
|
||
Started by seqadmin, 03-17-2023, 12:32 PM
|
0 responses
17 views
0 likes
|
Last Post
by seqadmin
03-17-2023, 12:32 PM
|
||
Started by seqadmin, 03-15-2023, 12:42 PM
|
0 responses
22 views
0 likes
|
Last Post
by seqadmin
03-15-2023, 12:42 PM
|
Leave a comment: