Monday, November 28, 2016

Native Media Network / Indian Country Books

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BOOK BUSTER HOLIDAY GIVEAWAY !!!!!

Purchase any Book Prior to Dec. 31st

Recieve a copy of Voice of Indigenous People FREEEE
Enter Coupon Code ICBFree


We are pleased to announce a major upgrade  to our platform with the introduction of  our book Catalog  www.indiancountrybooks.com  with a listing of over 10,000 titles of Native American Art, Biography, Ceremony, Culture,  Folk lore, History, Sovereignty  and Tribal heritage & traditions.  The collection of books represents to most complete catalog dedicated to Indian country.

Our plan for 2017 is to introduce a Tribal publishing program with a focus on cultural literacy and K12 educational material. 

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Friday, November 25, 2016

Fwd: Confirmed - Keynote Speaker for Clinical Genomics Track at BioITWorld 2017 this May 23-25 in Boston

I discuss how we interpret and prioritize the many variants in a personal genome. I concentrate on rare and somatic variants and discuss ways of assessing their impact in coding regions using protein structure. For non-coding regions, I present ways to analyze the overall burden of mutations, finding allelic elements differentially affected by variants in paternal and maternal chromosomes and using network connectivity to prioritize variants.

65 word edit
==
i0bioit17 

 


Thursday, November 17, 2016

Native Media Network / Indian Country Books

www.nativemedianetwork.com

To our viewers; thank you for your support !!!!

We are pleased to announce a major upgrade  to our platform with the introduction of  our book Catalog  www.indiancountrybooks.com  with a listing of over 10,000 titles of Native American Art, Biography, Ceremony, Culture,  Folk lore, History, Sovereignty  and Tribal heritage & traditions.  The collection of books represents to most complete catalog dedicated to Indian country.

Holiday Discount of 25% for all orders placed by December 31, 2016  * (Use Code ICB25)

 

Our plan for 2017 is to introduce a Tribal publishing program with a focus on cultural literacy and K12 educational material. 

Tune us in on www.NDN1.com for our 24/7  broadcast channel visit our archive tab  for previous live events.

Tweet us @ndn1talk
Facebook nativemedia
Email info@nativemedianetwork.com

Above all !!!!! forward this your friends  

Stand with Standing Rock - Support our Warriors

Monday, September 26, 2016

Abstract for talk at UNC Charlotte (Nov. 2016)

TITLE:

Personal Genomics

ABSTRACT:

My talk will focus on a variety of topics in personal genomics,
principally on how we interpret and prioritize the many variants in a
personal genome. I will concentrate on rare and somatic variants. I
will discuss a number of ways of assessing their impact in coding
regions using protein structure (via looking for cryptic allosteric
sites and regions of change in frustration). For non-coding regions,
I will present ways to analyze the overall burden of mutations,
finding allelic elements differentially affected by variants in
paternal and maternal chromosomes and using network connectivity (eg
hubs) to prioritize variants. Throughout the talk I will highlight a
number of practical software tools that we have developed for
prioritization, including: FunSeq.gersteinlab.org,
AlleleDB.gersteinlab.org, STRESS.gersteinlab.org and
Networks.gersteinlab.org . I will also motivate the talk a bit by
discussing why prioritization is useful in the context of rapidly
increasing amounts of genome sequences.

REFS

http://papers.gersteinlab.org/papers/alleledb
http://papers.gersteinlab.org/papers/stress
http://papers.gersteinlab.org/papers/costseq2
http://papers.gersteinlab.org/papers/larva
http://papers.gersteinlab.org/papers/music
http://papers.gersteinlab.org/papers/funseq
==

i0uncc16

Wednesday, September 21, 2016

Fwd: Abstract for talk at Ohio State for BMI seminar series (Oct. 2016)

Personal Genomics

My talk will focus on a variety of topics in personal genomics,
principally on how we interpret and prioritize the many variants in a
personal genome. I will concentrate on rare and somatic variants. I
will discuss a number of ways of assessing their impact in coding regions
using protein structure (via
looking for cryptic allosteric sites and regions of regions great
change in frustration).
For non-coding regions, I will present ways to analyze
the overall burden of mutations, finding allelic elements
differentially affected by variants in paternal and maternal alleles
and using network connectivity (eg hubs) to prioritize variants.
Throughout the talk I will
highlight a number of practical software tools that we have developed
for prioritization, including: FunSeq.gersteinlab.org ,
AlleleDB.gersteinlab.org, STRESS.gersteinlab.org and
Networks.gersteinlab.org . I will also motivate the talk a bit by
discussing why prioritization is useful in the context of rapidly
increasing amounts of genome sequences.

==
i0os16

Friday, September 9, 2016

Donation Award Notice

Dear Email Owner,

This is to inform you that you have been picked for a donation award sum of (US$1,500,000.00) One Million, Five Hundred Thousand United States Dollars by Buffett Foundation.

For more details regarding this donation,you are advised to contact the office of Warren Buffett today.

Respectfully Submitted,
Kelly Hayes
For Buffett Foundation

Thursday, September 1, 2016

Abstract for talk at Penn Bioinformatics Forum (Sep. 2016)

Personal Genomics

My talk will focus on a variety of topics in personal genomics,
principally on how we interpret and prioritize the many variants in a
personal genome. I will concentrate on rare and somatic variants. I
will discuss a number of ways of assessing their impact in coding regions
using protein structure (via
looking for cryptic allosteric sites and regions of regions great
change in frustration).
For non-coding regions, I will present ways to analyze
the overall burden of mutations, finding allelic elements
differentially affected by variants in paternal and maternal alleles
and using network connectivity (eg hubs) to prioritize variants.
Throughout the talk I will
highlight a number of practical software tools that we have developed
for prioritization, including: FunSeq.gersteinlab.org ,
AlleleDB.gersteinlab.org, STRESS.gersteinlab.org and
Networks.gersteinlab.org . I will also motivate the talk a bit by
discussing why prioritization is useful in the context of rapidly
increasing amounts of genome sequences.

==
i0pbf

Wednesday, August 31, 2016

Hello

Hello,

My name is Paul,i am from USA and i am an Engineer.

I lost my wife some years back and i have a daughter whom i cherish so much.I have been single and alone since then. I think this is my time to move on.

I am looking for woman who is honest and sincere in wanting a serious relationship,someone kind and caring, with a good sense of humor,someone who knows how to treat a man and make him feel that he is important to her.Most importantly,someone who does not lie or play head games.

Age or location is not a barrier.All i need is TRUE love.I am a happy person, responsible,honest, considerate, caring,sincere,serious and have a good sense of humor.Please let me know if you are interested in having a serious relationship with me.

I understand this is not the appropriate way or platform for such form of introduction, but i am only taking the chance to see if i will be lucky to get a response from you.

Am sorry if i invaded your private space. Apologies. I would be glad to share more about myself with you and send you some of my pictures.

With Love,

Paul

Friday, August 19, 2016

2016 SFNM1 Indian Market

Can't visit Santa Fe for the 2016 Indian Market ???
Not to worry, we will bring it to you

Log into www.sfnm1.com
on your Cell, Tab, PC or Web TV

 

Santa Fe Media Network  in collaboration with Tourism Santa Fe will be broadcasting select events and interviewing artists from the Santa Fe plaza  with a roving camera to capture the excitement, beauty, and diversity of Native Art that surrounds the premier event of Santa Fe, Indian Market.  You can view  the events live from August 18 - 21.
If you missed any of the action you can view it from our archives.

Log in to enter a two day stay in Santa Fe compliments of Santa Fe Tourism

Tweet us @santafetalk   Email us info@sfnm1.com

 

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Saturday, July 23, 2016

This Is My Second Letter To You!!

This Is My Second Letter To You.

I am contacting you again because you bear the surname credentials of a deceased client and therefore can present you as the beneficiary to the inheritance in the intent of the deceased since there is no written will "intestate" Our legal services aim to provide our private clients with a complete service; we are ready to prepare files, set-up and administer Trusts, carry out the Administration Of Estates, prepare and administer Powers of Attorney.

All papers will be processed in your acceptance. In your acceptance of this deal, kindly forward your letter of acceptance, your current telephone and fax numbers and a forwarding address to alan389sh@163.com to enable us file necessary documents at our High Court Probate division for the release of this sum of money in your favor.

Warm regards,

Alan 

Sunday, July 3, 2016

Abstract for Talk on Genomic Privacy at Birkbeck College in July 2016

Genomic Privacy

I will talk about Genomic Privacy in general and then in relation to a
specific application of RNA-seq data. In general, with every new
exciting development in genomics come the often
under-appreciated ethical, legal and social concerns. Particularly with
regard to issues of privacy, there are tradeoffs as the
technology continues to develop and the real-life applications of
genomics become more of a reality. Numerous technical solutions have
been proposed, but every technical safeguard is accompanied by
increased complications with analyzing and manipulating datasets.
Moreover, technical solutions invite both white-hat and black-hat
efforts of circumvention, making them less useful in the long-run.
I propose a multi-prong approach to dealing with privacy
issues in genomics that includes technical, regulatory and social
advances that will create an environment that both safeguards privacy,
prevents harms associated with a lack of privacy and promotes
innovation in the fields of genomics and medicine.

To illustrate the complex aspects of privacy, I go through two case
studies that inter-relate RNA-seq data (and functional genomics data,
in general) with variants. On one hand, scientists can use these data
to generate general conclusions; on the other hand it is interesting
and worthwhile to relate it to genetic variants. I go over some
aspects of private information leakage in dealing with RNA-seq,
particularly related to eQTLs. Then I describe aspects of RNA-seq
calculations that cannot be abstracted from variants -- particularly,
those related to allele-specific expression.

==
i0genc16+bida

Tuesday, June 28, 2016

Abstract & Title for talk at Royal Holloway, University of London (July 2016)

Personal Genomics

My talk will focus on a variety of topics in personal genomics,
principally on how we interpret and prioritize the many variants in a
personal genome. I will concentrate on rare and somatic variants. I
will discuss a number of ways of getting at their impact including
looking for cryptic allosteric sites in coding regions, analyzing the
burdening in non-coding regions, finding allelic elements
differentially affected by variants in paternal and maternal alleles
and using network connectivity (eg hubs). Throughout the talk I will
highlight a number of practical software tools that we have developed
for prioritization, including: FunSeq.gersteinlab.org ,
AlleleDB.gersteinlab.org, STRESS.gersteinlab.org and
Networks.gersteinlab.org . I will also motivate the talk a bit by
discussing why prioritization is useful in the context of rapidly
increasing amounts of genome sequences.

==
i0genc16+rh

Saturday, April 23, 2016

Fwd: Abstract for Talk on Personal Genomics

Abstract & Title for talk at Big Data Bioinformatics (May 2016, Boston, MA)

Personal Genomics

My talk will focus on a variety of topics in personal genomics,
principally on how we interpret and prioritize the many variants in a
personal genome. I will concentrate on rare and somatic variants. I
will discuss a number of ways of getting at the impact of rare
variants including looking for cryptic allosteric sites in coding
regions, analyzing the burdening in non-coding regions, finding
allelic elements differentially affected by variants in paternal and
maternal alleles and using at network connectivity (eg hubs).
Throughout the talk I will highlight a number of practical software
tools that we have developed for this purpose, including:
FunSeq.gersteinlab.org , AlleleDB.gersteinlab.org ,
STRESS.gersteinlab.org and Networks.gersteinlab.org .

==
i0gtcbio

Saturday, April 9, 2016

Re: ModSTI: Conference Abstract

Abstract:

The emergence of collective creative enterprise such as large
scientific consortia is a unique feature in modern scientific
research, especially in genomic areas. Recent examples include the
ENCyclopedia Of DNA Elements (ENCODE) consortium annotating the human
genome and the 1000 Genomes consortium generating a catalog of
uniformly called variants for the biomedical community. To ensure that
the scientific community can benefit from these efforts, it is
important to understand the connections between consortium members and
researchers outside of the consortium. To address the issue, we
analyzed the temporal co-authorship network structures of ENCODE and
modENCODE consortia. Our analysis revealed their publication
patterns showing that the consortium members work closely as a
community whereas non-members collaborate in the scale of a few
laboratories. We also identified a few brokers playing an important
role to facilitate collaborations with outside researchers, which
suggests that large scientific consortia should set up formal an
outreach group to communicate with outside researchers.

Daifeng Wang, Koon-Kiu Yan, Joel Rozowsky, Eric Pan, Mark
Gerstein, Temporal dynamics of collaborative networks driven by large
scientific consortia, Trends in Genetics, 2016
http://dx.doi.org/10.1016/j.tig.2016.02.006
==
i0scisipc