Transcript copy number estimation using a mouse whole-genome oligonucleotide microarray.

Abstract:

:The ability to quantitatively measure the expression of all genes in a given tissue or cell with a single assay is an exciting promise of gene-expression profiling technology. An in situ-synthesized 60-mer oligonucleotide microarray designed to detect transcripts from all mouse genes was validated, as well as a set of exogenous RNA controls derived from the yeast genome (made freely available without restriction), which allow quantitative estimation of absolute endogenous transcript abundance.

journal_name

Genome Biol

journal_title

Genome biology

authors

Carter MG,Sharov AA,VanBuren V,Dudekula DB,Carmack CE,Nelson C,Ko MS

doi

10.1186/gb-2005-6-7-r61

keywords:

subject

Has Abstract

pub_date

2005-01-01 00:00:00

pages

R61

issue

7

eissn

1474-7596

issn

1474-760X

pii

gb-2005-6-7-r61

journal_volume

6

pub_type

杂志文章
  • Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome.

    abstract:BACKGROUND:The functional impact of genetic variation has been extensively surveyed, revealing that genetic changes correlated to phenotypes lie mostly in non-coding genomic regions. Studies have linked allele-specific genetic changes to gene expression, DNA methylation, and histone marks but these investigations have ...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/s13059-017-1173-7

    authors: Cheung WA,Shao X,Morin A,Siroux V,Kwan T,Ge B,Aïssi D,Chen L,Vasquez L,Allum F,Guénard F,Bouzigon E,Simon MM,Boulier E,Redensek A,Watt S,Datta A,Clarke L,Flicek P,Mead D,Paul DS,Beck S,Bourque G,Lathrop M,

    更新日期:2017-03-10 00:00:00

  • The promise and limitations of population exomics for human evolution studies.

    abstract::Exome sequencing is poised to yield substantial insights into human genetic variation and evolutionary history, but there are significant challenges to overcome before this becomes a reality. ...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/gb-2011-12-9-127

    authors: Tennessen JA,O'Connor TD,Bamshad MJ,Akey JM

    更新日期:2011-09-14 00:00:00

  • Selection in the evolution of gene duplications.

    abstract:BACKGROUND:Gene duplications have a major role in the evolution of new biological functions. Theoretical studies often assume that a duplication per se is selectively neutral and that, following a duplication, one of the gene copies is freed from purifying (stabilizing) selection, which creates the potential for evolut...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/gb-2002-3-2-research0008

    authors: Kondrashov FA,Rogozin IB,Wolf YI,Koonin EV

    更新日期:2002-01-01 00:00:00

  • Reduced intrinsic DNA curvature leads to increased mutation rate.

    abstract:BACKGROUND:Mutation rates vary across the genome. Many trans factors that influence mutation rates have been identified, as have specific sequence motifs at the 1-7-bp scale, but cis elements remain poorly characterized. The lack of understanding regarding why different sequences have different mutation rates hampers o...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/s13059-018-1525-y

    authors: Duan C,Huan Q,Chen X,Wu S,Carey LB,He X,Qian W

    更新日期:2018-09-14 00:00:00

  • Gene editing of the multi-copy H2A.B gene and its importance for fertility.

    abstract:BACKGROUND:Altering the biochemical makeup of chromatin by the incorporation of histone variants during development represents a key mechanism in regulating gene expression. The histone variant H2A.B, H2A.B.3 in mice, appeared late in evolution and is most highly expressed in the testis. In the mouse, it is encoded by ...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/s13059-019-1633-3

    authors: Anuar ND,Kurscheid S,Field M,Zhang L,Rebar E,Gregory P,Buchou T,Bowles J,Koopman P,Tremethick DJ,Soboleva TA

    更新日期:2019-01-31 00:00:00

  • Transposons as tools for enhancer trap screens in vertebrates.

    abstract::DNA transposons are efficient tools in transgenesis and have therefore become popular in the analysis of the regulatory genome in vertebrates via enhancer trap screens. Here, I discuss recent progress in this field of research, with a focus on the application of one of these transposons, namely the medaka fish derived...

    journal_title:Genome biology

    pub_type: 杂志文章,评审

    doi:10.1186/gb-2007-8-s1-s8

    authors: Korzh V

    更新日期:2007-01-01 00:00:00

  • Single-cell RNA-seq transcriptome analysis of linear and circular RNAs in mouse preimplantation embryos.

    abstract::Circular RNAs (circRNAs) are a new class of non-polyadenylated non-coding RNAs that may play important roles in many biological processes. Here we develop a single-cell universal poly(A)-independent RNA sequencing (SUPeR-seq) method to sequence both polyadenylated and non-polyadenylated RNAs from individual cells. Thi...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/s13059-015-0706-1

    authors: Fan X,Zhang X,Wu X,Guo H,Hu Y,Tang F,Huang Y

    更新日期:2015-07-23 00:00:00

  • Avianbase: a community resource for bird genomics.

    abstract::Giving access to sequence and annotation data for genome assemblies is important because, while facilitating research, it places both assembly and annotation quality under scrutiny, resulting in improvements to both. Therefore we announce Avianbase, a resource for bird genomics, which provides access to data released ...

    journal_title:Genome biology

    pub_type: 信件

    doi:10.1186/s13059-015-0588-2

    authors: Eöry L,Gilbert MT,Li C,Li B,Archibald A,Aken BL,Zhang G,Jarvis E,Flicek P,Burt DW

    更新日期:2015-01-29 00:00:00

  • Zinc finger nuclease-based double-strand breaks attenuate malaria parasites and reveal rare microhomology-mediated end joining.

    abstract:BACKGROUND:Genome editing of malaria parasites is key to the generation of live attenuated parasites used in experimental vaccination approaches. DNA repair in Plasmodium generally occurs only through homologous recombination. This has been used to generate transgenic parasites that lack one to three genes, leading to ...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/s13059-015-0811-1

    authors: Singer M,Marshall J,Heiss K,Mair GR,Grimm D,Mueller AK,Frischknecht F

    更新日期:2015-11-17 00:00:00

  • A physical map for the Amborella trichopoda genome sheds light on the evolution of angiosperm genome structure.

    abstract:BACKGROUND:Recent phylogenetic analyses have identified Amborella trichopoda, an understory tree species endemic to the forests of New Caledonia, as sister to a clade including all other known flowering plant species. The Amborella genome is a unique reference for understanding the evolution of angiosperm genomes becau...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/gb-2011-12-5-r48

    authors: Zuccolo A,Bowers JE,Estill JC,Xiong Z,Luo M,Sebastian A,Goicoechea JL,Collura K,Yu Y,Jiao Y,Duarte J,Tang H,Ayyampalayam S,Rounsley S,Kudrna D,Paterson AH,Pires JC,Chanderbali A,Soltis DE,Chamala S,Barbazuk B,So

    更新日期:2011-01-01 00:00:00

  • Probing the yeast proteome for RNA-processing factors.

    abstract::A method has been developed to identify proteins required for the biogenesis of non-coding RNA in yeast, using a microarray to screen for aberrant patterns of RNA processing in mutant strains, and new proteins involved in the processing of ribosomal and non-coding RNAs have been found. ...

    journal_title:Genome biology

    pub_type: 杂志文章,评审

    doi:10.1186/gb-2003-4-10-229

    authors: Granneman S,Baserga SJ

    更新日期:2003-01-01 00:00:00

  • Genomes of uncultured eukaryotes: sorting FACS from fiction.

    abstract::A recent study explores the genome content of uncultured unicellular marine eukaryotes and provides insights about interactions between uncultured eukaryotes and other biological entities. ...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/gb-2011-12-6-117

    authors: Worden AZ,Dupont C,Allen AE

    更新日期:2011-06-27 00:00:00

  • Transcriptional profiling of long non-coding RNAs and novel transcribed regions across a diverse panel of archived human cancers.

    abstract:BACKGROUND:Molecular characterization of tumors has been critical for identifying important genes in cancer biology and for improving tumor classification and diagnosis. Long non-coding RNAs, as a new, relatively unstudied class of transcripts, provide a rich opportunity to identify both functional drivers and cancer-t...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/gb-2012-13-8-r75

    authors: Brunner AL,Beck AH,Edris B,Sweeney RT,Zhu SX,Li R,Montgomery K,Varma S,Gilks T,Guo X,Foley JW,Witten DM,Giacomini CP,Flynn RA,Pollack JR,Tibshirani R,Chang HY,van de Rijn M,West RB

    更新日期:2012-08-28 00:00:00

  • Modular organization in the reductive evolution of protein-protein interaction networks.

    abstract:BACKGROUND:The variation in the sizes of the genomes of distinct life forms remains somewhat puzzling. The organization of proteins into domains and the different mechanisms that regulate gene expression are two factors that potentially increase the capacity of genomes to create more complex systems. High-throughput pr...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/gb-2007-8-5-r94

    authors: Tamames J,Moya A,Valencia A

    更新日期:2007-01-01 00:00:00

  • Genome-wide analyses of Shavenbaby target genes reveals distinct features of enhancer organization.

    abstract:BACKGROUND:Developmental programs are implemented by regulatory interactions between Transcription Factors (TFs) and their target genes, which remain poorly understood. While recent studies have focused on regulatory cascades of TFs that govern early development, little is known about how the ultimate effectors of cell...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/gb-2013-14-8-r86

    authors: Menoret D,Santolini M,Fernandes I,Spokony R,Zanet J,Gonzalez I,Latapie Y,Ferrer P,Rouault H,White KP,Besse P,Hakim V,Aerts S,Payre F,Plaza S

    更新日期:2013-08-23 00:00:00

  • Single-cell sequencing reveals karyotype heterogeneity in murine and human malignancies.

    abstract:BACKGROUND:Chromosome instability leads to aneuploidy, a state in which cells have abnormal numbers of chromosomes, and is found in two out of three cancers. In a chromosomal instable p53 deficient mouse model with accelerated lymphomagenesis, we previously observed whole chromosome copy number changes affecting all ly...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/s13059-016-0971-7

    authors: Bakker B,Taudt A,Belderbos ME,Porubsky D,Spierings DC,de Jong TV,Halsema N,Kazemier HG,Hoekstra-Wakker K,Bradley A,de Bont ES,van den Berg A,Guryev V,Lansdorp PM,Colomé-Tatché M,Foijer F

    更新日期:2016-05-31 00:00:00

  • Mathematical models in mammalian cell biology.

    abstract::A report on the Conference on Systems Biology of Mammalian Cells, Dresden, Germany, 22-24 May 2008. ...

    journal_title:Genome biology

    pub_type:

    doi:10.1186/gb-2008-9-7-316

    authors: Herzel H,Blüthgen N

    更新日期:2008-01-01 00:00:00

  • The MAP1 family of microtubule-associated proteins.

    abstract::MAP1-family proteins are classical microtubule-associated proteins (MAPs) that bind along the microtubule lattice. The founding members, MAP1A and MAP1B, are predominantly expressed in neurons, where they are thought to be important in the formation and development of axons and dendrites. Mammalian genomes usually con...

    journal_title:Genome biology

    pub_type: 杂志文章,评审

    doi:10.1186/gb-2006-7-6-224

    authors: Halpain S,Dehmelt L

    更新日期:2006-01-01 00:00:00

  • PU.1 target genes undergo Tet2-coupled demethylation and DNMT3b-mediated methylation in monocyte-to-osteoclast differentiation.

    abstract:BACKGROUND:DNA methylation is a key epigenetic mechanism for driving and stabilizing cell-fate decisions. Local deposition and removal of DNA methylation are tightly coupled with transcription factor binding, although the relationship varies with the specific differentiation process. Conversion of monocytes to osteocla...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/gb-2013-14-9-r99

    authors: de la Rica L,Rodríguez-Ubreva J,García M,Islam AB,Urquiza JM,Hernando H,Christensen J,Helin K,Gómez-Vaquero C,Ballestar E

    更新日期:2013-01-01 00:00:00

  • VlincRNAs controlled by retroviral elements are a hallmark of pluripotency and cancer.

    abstract:BACKGROUND:The function of the non-coding portion of the human genome remains one of the most important questions of our time. Its vast complexity is exemplified by the recent identification of an unusual and notable component of the transcriptome - very long intergenic non-coding RNAs, termed vlincRNAs. RESULTS:Here ...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/gb-2013-14-7-r73

    authors: St Laurent G,Shtokalo D,Dong B,Tackett MR,Fan X,Lazorthes S,Nicolas E,Sang N,Triche TJ,McCaffrey TA,Xiao W,Kapranov P

    更新日期:2013-07-22 00:00:00

  • Genetic analysis of the human infective trypanosome Trypanosoma brucei gambiense: chromosomal segregation, crossing over, and the construction of a genetic map.

    abstract:BACKGROUND:Trypanosoma brucei is the causative agent of human sleeping sickness and animal trypanosomiasis in sub-Saharan Africa, and it has been subdivided into three subspecies: Trypanosoma brucei gambiense and Trypanosoma brucei rhodesiense, which cause sleeping sickness in humans, and the nonhuman infective Trypano...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/gb-2008-9-6-r103

    authors: Cooper A,Tait A,Sweeney L,Tweedie A,Morrison L,Turner CM,MacLeod A

    更新日期:2008-01-01 00:00:00

  • Detection and analysis of alternative splicing in Yarrowia lipolytica reveal structural constraints facilitating nonsense-mediated decay of intron-retaining transcripts.

    abstract:BACKGROUND:Hemiascomycetous yeasts have intron-poor genomes with very few cases of alternative splicing. Most of the reported examples result from intron retention in Saccharomyces cerevisiae and some have been shown to be functionally significant. Here we used transcriptome-wide approaches to evaluate the mechanisms u...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/gb-2010-11-6-r65

    authors: Mekouar M,Blanc-Lenfle I,Ozanne C,Da Silva C,Cruaud C,Wincker P,Gaillardin C,Neuvéglise C

    更新日期:2010-01-01 00:00:00

  • Personal genomes and precision medicine.

    abstract::A report of the fifth annual Personal Genomes and Medical Genomics meeting, held at Cold Spring Harbor Laboratory, Cold Spring Harbor, New York, USA, November 14-17, 2012. ...

    journal_title:Genome biology

    pub_type:

    doi:10.1186/gb-2012-13-12-324

    authors: Highnam G,Mittelman D

    更新日期:2012-12-19 00:00:00

  • Prediction of synergistic transcription factors by function conservation.

    abstract:BACKGROUND:Previous methods employed for the identification of synergistic transcription factors (TFs) are based on either TF enrichment from co-regulated genes or phylogenetic footprinting. Despite the success of these methods, both have limitations. RESULTS:We propose a new strategy to identify synergistic TFs by fu...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/gb-2007-8-12-r257

    authors: Hu Z,Hu B,Collins JF

    更新日期:2007-01-01 00:00:00

  • The continuum of causality in human genetic disorders.

    abstract::Studies of human genetic disorders have traditionally followed a reductionist paradigm. Traits are defined as Mendelian or complex based on family pedigree and population data, whereas alleles are deemed rare, common, benign, or deleterious based on their population frequencies. The availability of exome and genome da...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/s13059-016-1107-9

    authors: Katsanis N

    更新日期:2016-11-17 00:00:00

  • Genome-wide mapping of FOXM1 binding reveals co-binding with estrogen receptor alpha in breast cancer cells.

    abstract:BACKGROUND:The forkhead transcription factor FOXM1 is a key regulator of the cell cycle. It is frequently over-expressed in cancer and is emerging as an important therapeutic target. In breast cancer FOXM1 expression is linked with estrogen receptor (ERα) activity and resistance to endocrine therapies, with high levels...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/gb-2013-14-1-r6

    authors: Sanders DA,Ross-Innes CS,Beraldi D,Carroll JS,Balasubramanian S

    更新日期:2013-01-24 00:00:00

  • Moving beyond genome sequencing into personalized genomic medicine: biological and computing challenges.

    abstract::A report of the second annual Beyond the Genome conference held on the 19-22 September 2011 at The Universities at Shady Grove, Rockville, Maryland, USA, where increases in computing that may help make personal genomics a reality were a major focus. ...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/gb-2011-12-10-308

    authors: Kristensen DM

    更新日期:2011-10-24 00:00:00

  • Independent centromere formation in a capricious, gene-free domain of chromosome 13q21 in Old World monkeys and pigs.

    abstract:BACKGROUND:Evolutionary centromere repositioning and human analphoid neocentromeres occurring in clinical cases are, very likely, two stages of the same phenomenon whose properties still remain substantially obscure. Chromosome 13 is the chromosome with the highest number of neocentromeres. We reconstructed the mammali...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/gb-2006-7-10-r91

    authors: Cardone MF,Alonso A,Pazienza M,Ventura M,Montemurro G,Carbone L,de Jong PJ,Stanyon R,D'Addabbo P,Archidiacono N,She X,Eichler EE,Warburton PE,Rocchi M

    更新日期:2006-01-01 00:00:00

  • Crucial timing in schizophrenia: role of DNA methylation in early neurodevelopment.

    abstract::An exciting recent study examining the methylation profile of human brain tissue implicates early-life epigenetic disruption in the neurodevelopmental origin of schizophrenia. ...

    journal_title:Genome biology

    pub_type: 评论,杂志文章

    doi:10.1186/s13059-014-0495-y

    authors: Ryan J,Saffery R

    更新日期:2014-10-29 00:00:00

  • Genomic analysis of the domestication and post-Spanish conquest evolution of the llama and alpaca.

    abstract:BACKGROUND:Despite their regional economic importance and being increasingly reared globally, the origins and evolution of the llama and alpaca remain poorly understood. Here we report reference genomes for the llama, and for the guanaco and vicuña (their putative wild progenitors), compare these with the published alp...

    journal_title:Genome biology

    pub_type: 杂志文章

    doi:10.1186/s13059-020-02080-6

    authors: Fan R,Gu Z,Guang X,Marín JC,Varas V,González BA,Wheeler JC,Hu Y,Li E,Sun X,Yang X,Zhang C,Gao W,He J,Munch K,Corbett-Detig R,Barbato M,Pan S,Zhan X,Bruford MW,Dong C

    更新日期:2020-07-02 00:00:00