Anonymous ID: 482c3b Oct. 28, 2021, 7:34 p.m. No.14876245   🗄️.is 🔗kun   >>6261

>>14876207

 

Phylogenetic analysis of gene expression

Casey W Dunn 1 , Xi Luo, Zhijin Wu

Affiliations

 

PMID: 23748631 PMCID: PMC3796711 DOI: 10.1093/icb/ict068

 

Free PMC article

Abstract

 

Phylogenetic analyses of gene expression have great potential for addressing a wide range of questions. These analyses will, for example, identify genes that have evolutionary shifts in expression that are correlated with evolutionary changes in morphological, physiological, and developmental characters of interest. This will provide entirely new opportunities to identify genes related to particular phenotypes. There are, however, 3 key challenges that must be addressed for such studies to realize their potential. First, data on gene expression must be measured from multiple species, some of which may be field-collected, and parameterized in such a way that they can be compared across species. Second, it will be necessary to develop comparative phylogenetic methods suitable for large multidimensional datasets. In most phylogenetic comparative studies to date, the number n of independent observations (independent contrasts) has been greater than the number p of variables (characters). The behavior of comparative methods for these classic problems is now well understood under a wide variety of conditions. In studies of gene expression, and in studies based on other high-throughput tools, the number n of samples is dwarfed by the number p of variables. The estimated covariance matrices will be singular, complicating their analysis and interpretation, and prone to spurious results. Third, new approaches are needed to investigate the expression of the many genes whose phylogenies are not congruent with species phylogenies due to gene loss, gene duplication, and incomplete lineage sorting. Here we outline general considerations of project design for phylogenetic analyses of gene expression and suggest solutions to these three categories of challenges. These topics are relevant to high-throughput phenotypic data well beyond gene expression.

 

 

3662

07-Dec-2019 10:05:46 AM PSTQ !!Hs1Jq13jV68kun/projectdcomms103

 

Knowledge is power.

 

Think for yourself.

 

Trust yourself.

 

Do due diligence.

 

You awake, and thinking for yourself, is their greatest fear.

 

Sheep no more.

 

THE GREAT AWAKENING.

 

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Anonymous ID: 482c3b Oct. 28, 2021, 7:53 p.m. No.14876391   🗄️.is 🔗kun

2557

05-Dec-2018 2:47:00 PM PSTQ !!mG7VJxZNCI8ch/qresearch

Archived links:

 

1

 

https://thehill.com/hilltv/rising/419901-fbi-email-chain-may-provide-most-damning-evidence-of-fisa-abuses-yet

 

What do you want for XMAS?

 

Q

 

Happy B-Day, Q?????

 

Born Sally Caroline Quillian

 

1960 (age 60–61)

Atlanta, Georgia, U.S.

 

 

Sally Quillian Yates (born Sally Caroline Quillian; 1960) is an American lawyer. From 2010 to 2015, she was United States Attorney for the Northern District of Georgia. In 2015, she was appointed United States Deputy Attorney General by President Barack Obama. Following the inauguration of President Donald Trump and the departure of Attorney General Loretta Lynch on January 20, 2017, Yates served as Acting Attorney General for 10 days.