SNP-based quantitative deconvolution of biological mixtures: application to the detection of cows with subclinical mastitis by whole-genome sequencing of tank milk.

Abstract:

:Biological products of importance in food (e.g., milk) and medical (e.g., donor blood-derived products) sciences often correspond to mixtures of samples contributed by multiple individuals. Identifying which individuals contributed to the mixture and in what proportions may be of interest in several circumstances. We herein present a method that allows to do this by shallow whole-genome sequencing of the DNA in mixed samples from hundreds of donors. We show the efficacy of the approach for the detection of cows with subclinical mastitis by analysis of farms' tank mixtures containing milk from as many as 500 cows.

journal_name

Genome Res

journal_title

Genome research

authors

Coppieters W,Karim L,Georges M

doi

10.1101/gr.256172.119

subject

Has Abstract

pub_date

2020-08-01 00:00:00

pages

1201-1207

issue

8

eissn

1088-9051

issn

1549-5469

pii

gr.256172.119

journal_volume

30

pub_type

杂志文章
  • A method for detecting IBD regions simultaneously in multiple individuals--with applications to disease genetics.

    abstract::All individuals in a finite population are related if traced back long enough and will, therefore, share regions of their genomes identical by descent (IBD). Detection of such regions has several important applications-from answering questions about human evolution to locating regions in the human genome containing di...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.115360.110

    authors: Moltke I,Albrechtsen A,Hansen TV,Nielsen FC,Nielsen R

    更新日期:2011-07-01 00:00:00

  • A platform for curated products from novel open reading frames prompts reinterpretation of disease variants.

    abstract::Recent evidence from proteomics and deep massively parallel sequencing studies have revealed that eukaryotic genomes contain substantial numbers of as-yet-uncharacterized open reading frames (ORFs). We define these uncharacterized ORFs as novel ORFs (nORFs). nORFs in humans are mostly under 100 codons and are found in...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.263202.120

    authors: Neville MDC,Kohze R,Erady C,Meena N,Hayden M,Cooper DN,Mort M,Prabakaran S

    更新日期:2021-01-19 00:00:00

  • Novel noncoding RNA from human Y distal heterochromatic block (Yq12) generates testis-specific chimeric CDC2L2.

    abstract::The human Y chromosome, because it is enriched in repetitive DNA, has been very intractable to genetic and molecular analyses. There is no previous evidence for developmental stage- and testis-specific transcription from the male-specific region of the Y (MSY). Here, we present evidence for the first time for a develo...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.5155706

    authors: Jehan Z,Vallinayagam S,Tiwari S,Pradhan S,Singh L,Suresh A,Reddy HM,Ahuja YR,Jesudasan RA

    更新日期:2007-04-01 00:00:00

  • Polycomb preferentially targets stalled promoters of coding and noncoding transcripts.

    abstract::The Polycomb group (PcG) and Trithorax group (TrxG) of proteins are required for stable and heritable maintenance of repressed and active gene expression states. Their antagonistic function on gene control, repression for PcG and activity for TrxG, is mediated by binding to chromatin and subsequent epigenetic modifica...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.114348.110

    authors: Enderle D,Beisel C,Stadler MB,Gerstung M,Athri P,Paro R

    更新日期:2011-02-01 00:00:00

  • Systematic recovery and analysis of full-ORF human cDNA clones.

    abstract::The Mammalian Gene Collection (MGC) consortium (http://mgc.nci.nih.gov) seeks to establish publicly available collections of full-ORF cDNAs for several organisms of significance to biomedical research, including human. To date over 15,200 human cDNA clones containing full-length open reading frames (ORFs) have been id...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.2473704

    authors: Baross A,Butterfield YS,Coughlin SM,Zeng T,Griffith M,Griffith OL,Petrescu AS,Smailus DE,Khattra J,McDonald HL,McKay SJ,Moksa M,Holt RA,Marra MA

    更新日期:2004-10-01 00:00:00

  • The portability of tagSNPs across populations: a worldwide survey.

    abstract::In the search for common genetic variants that contribute to prevalent human diseases, patterns of linkage disequilibrium (LD) among linked markers should be considered when selecting SNPs. Genotyping efficiency can be increased by choosing tagging SNPs (tagSNPs) in LD with other SNPs. However, it remains to be seen w...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.4138406

    authors: González-Neira A,Ke X,Lao O,Calafell F,Navarro A,Comas D,Cann H,Bumpstead S,Ghori J,Hunt S,Deloukas P,Dunham I,Cardon LR,Bertranpetit J

    更新日期:2006-03-01 00:00:00

  • Relationship between histone modifications and transcription factor binding is protein family specific.

    abstract::The very small fraction of putative binding sites (BSs) that are occupied by transcription factors (TFs) in vivo can be highly variable across different cell types. This observation has been partly attributed to changes in chromatin accessibility and histone modification (HM) patterns surrounding BSs. Previous studies...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.220079.116

    authors: Xin B,Rohs R

    更新日期:2018-01-11 00:00:00

  • Prokaryotic phylogenies inferred from protein structural domains.

    abstract::The determination of the phylogenetic relationships among microorganisms has long relied primarily on gene sequence information. Given that prokaryotic organisms often lack morphological characteristics amenable to phylogenetic analysis, prokaryotic phylogenies, in particular, are often based on sequence data. In this...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.3033805

    authors: Deeds EJ,Hennessey H,Shakhnovich EI

    更新日期:2005-03-01 00:00:00

  • The origins and evolution of chromosomes, dosage compensation, and mechanisms underlying venom regulation in snakes.

    abstract::Here we use a chromosome-level genome assembly of a prairie rattlesnake (Crotalus viridis), together with Hi-C, RNA-seq, and whole-genome resequencing data, to study key features of genome biology and evolution in reptiles. We identify the rattlesnake Z Chromosome, including the recombining pseudoautosomal region, and...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.240952.118

    authors: Schield DR,Card DC,Hales NR,Perry BW,Pasquesi GM,Blackmon H,Adams RH,Corbin AB,Smith CF,Ramesh B,Demuth JP,Betrán E,Tollis M,Meik JM,Mackessy SP,Castoe TA

    更新日期:2019-04-01 00:00:00

  • An assessment of gene prediction accuracy in large DNA sequences.

    abstract::One of the first useful products from the human genome will be a set of predicted genes. Besides its intrinsic scientific interest, the accuracy and completeness of this data set is of considerable importance for human health and medicine. Though progress has been made on computational gene identification in terms of ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.122800

    authors: Guigó R,Agarwal P,Abril JF,Burset M,Fickett JW

    更新日期:2000-10-01 00:00:00

  • Genomic organization of TEL: the human ETS-variant gene 6.

    abstract::We have constructed a detailed map of the genomic region containing the ETS-variant gene 6 (ETV6), involved in translocations and deletions associated with hematologic malignancies. Thirty-eight cosmids were characterized belonging to two contigs spanning 340 kb, and an EcoRl restriction map was developed. The gap bet...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.6.5.404

    authors: Baens M,Peeters P,Guo C,Aerssens J,Marynen P

    更新日期:1996-05-01 00:00:00

  • Retroelement distributions in the human genome: variations associated with age and proximity to genes.

    abstract::Remnants of more than 3 million transposable elements, primarily retroelements, comprise nearly half of the human genome and have generated much speculation concerning their evolutionary significance. We have exploited the draft human genome sequence to examine the distributions of retroelements on a genome-wide scale...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.388902

    authors: Medstrand P,van de Lagemaat LN,Mager DL

    更新日期:2002-10-01 00:00:00

  • Comparative methylome analysis of benign and malignant peripheral nerve sheath tumors.

    abstract::Aberrant DNA methylation (DNAm) was first linked to cancer over 25 yr ago. Since then, many studies have associated hypermethylation of tumor suppressor genes and hypomethylation of oncogenes to the tumorigenic process. However, most of these studies have been limited to the analysis of promoters and CpG islands (CGIs...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.109678.110

    authors: Feber A,Wilson GA,Zhang L,Presneau N,Idowu B,Down TA,Rakyan VK,Noon LA,Lloyd AC,Stupka E,Schiza V,Teschendorff AE,Schroth GP,Flanagan A,Beck S

    更新日期:2011-04-01 00:00:00

  • GrapeTree: visualization of core genomic relationships among 100,000 bacterial pathogens.

    abstract::Current methods struggle to reconstruct and visualize the genomic relationships of large numbers of bacterial genomes. GrapeTree facilitates the analyses of large numbers of allelic profiles by a static "GrapeTree Layout" algorithm that supports interactive visualizations of large trees within a web browser window. Gr...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.232397.117

    authors: Zhou Z,Alikhan NF,Sergeant MJ,Luhmann N,Vaz C,Francisco AP,Carriço JA,Achtman M

    更新日期:2018-09-01 00:00:00

  • Global analysis of protein homomerization in Saccharomyces cerevisiae.

    abstract::In vivo analyses of the occurrence, subcellular localization, and dynamics of protein-protein interactions (PPIs) are important issues in functional proteomic studies. The bimolecular fluorescence complementation (BiFC) assay has many advantages in that it provides a reliable way to detect PPIs in living cells with mi...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.231860.117

    authors: Kim Y,Jung JP,Pack CG,Huh WK

    更新日期:2019-01-01 00:00:00

  • HERC2 rs12913832 modulates human pigmentation by attenuating chromatin-loop formation between a long-range enhancer and the OCA2 promoter.

    abstract::Pigmentation of skin, eye, and hair reflects some of the most evident common phenotypes in humans. Several candidate genes for human pigmentation are identified. The SNP rs12913832 has strong statistical association with human pigmentation. It is located within an intron of the nonpigment gene HERC2, 21 kb upstream of...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.128652.111

    authors: Visser M,Kayser M,Palstra RJ

    更新日期:2012-03-01 00:00:00

  • Arabidopsis-rice: will colinearity allow gene prediction across the eudicot-monocot divide?

    abstract::With the genomic sequencing of Arabidopsis nearing completion and rice sequencing very much in its infancy, a key question is whether we can exploit the Arabidopsis sequence to identify candidate genes for traits in cereal crops using a map-based approach. This requires the existence of colinearity between the Arabido...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.9.9.825

    authors: Devos KM,Beales J,Nagamura Y,Sasaki T

    更新日期:1999-09-01 00:00:00

  • Characterizing the genetic basis of transcriptome diversity through RNA-sequencing of 922 individuals.

    abstract::Understanding the consequences of regulatory variation in the human genome remains a major challenge, with important implications for understanding gene regulation and interpreting the many disease-risk variants that fall outside of protein-coding regions. Here, we provide a direct window into the regulatory consequen...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.155192.113

    authors: Battle A,Mostafavi S,Zhu X,Potash JB,Weissman MM,McCormick C,Haudenschild CD,Beckman KB,Shi J,Mei R,Urban AE,Montgomery SB,Levinson DF,Koller D

    更新日期:2014-01-01 00:00:00

  • Sequences of 95 human MHC haplotypes reveal extreme coding variation in genes other than highly polymorphic HLA class I and II.

    abstract::The most polymorphic part of the human genome, the MHC, encodes over 160 proteins of diverse function. Half of them, including the HLA class I and II genes, are directly involved in immune responses. Consequently, the MHC region strongly associates with numerous diseases and clinical therapies. Notoriously, the MHC re...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.213538.116

    authors: Norman PJ,Norberg SJ,Guethlein LA,Nemat-Gorgani N,Royce T,Wroblewski EE,Dunn T,Mann T,Alicata C,Hollenbach JA,Chang W,Shults Won M,Gunderson KL,Abi-Rached L,Ronaghi M,Parham P

    更新日期:2017-05-01 00:00:00

  • Single-cell sequencing data reveal widespread recurrence and loss of mutational hits in the life histories of tumors.

    abstract::Intra-tumor heterogeneity poses substantial challenges for cancer treatment. A tumor's composition can be deduced by reconstructing its mutational history. Central to current approaches is the infinite sites assumption that every genomic position can only mutate once over the lifetime of a tumor. The validity of this ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.220707.117

    authors: Kuipers J,Jahn K,Raphael BJ,Beerenwinkel N

    更新日期:2017-11-01 00:00:00

  • Parente2: a fast and accurate method for detecting identity by descent.

    abstract::Identity-by-descent (IBD) inference is the problem of establishing a genetic connection between two individuals through a genomic segment that is inherited by both individuals from a recent common ancestor. IBD inference is an important preceding step in a variety of population genomic studies, ranging from demographi...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.173641.114

    authors: Rodriguez JM,Bercovici S,Huang L,Frostig R,Batzoglou S

    更新日期:2015-02-01 00:00:00

  • Automatic analysis of dividing cells in live cell movies to detect mitotic delays and correlate phenotypes in time.

    abstract::Live-cell imaging allows detailed dynamic cellular phenotyping for cell biology and, in combination with small molecule or drug libraries, for high-content screening. Fully automated analysis of live cell movies has been hampered by the lack of computational approaches that allow tracking and recognition of individual...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.092494.109

    authors: Harder N,Mora-Bermúdez F,Godinez WJ,Wünsche A,Eils R,Ellenberg J,Rohr K

    更新日期:2009-11-01 00:00:00

  • Transcription factor binding and modified histones in human bidirectional promoters.

    abstract::Bidirectional promoters have received considerable attention because of their ability to regulate two downstream genes (divergent genes). They are also highly abundant, directing the transcription of approximately 11% of genes in the human genome. We categorized the presence of DNA sequence motifs, binding of transcri...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.5623407

    authors: Lin JM,Collins PJ,Trinklein ND,Fu Y,Xi H,Myers RM,Weng Z

    更新日期:2007-06-01 00:00:00

  • Phenotypically distinct female castes in honey bees are defined by alternative chromatin states during larval development.

    abstract::The capacity of the honey bee to produce three phenotypically distinct organisms (two female castes; queens and sterile workers, and haploid male drones) from one genotype represents one of the most remarkable examples of developmental plasticity in any phylum. The queen-worker morphological and reproductive divide is...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.236497.118

    authors: Wojciechowski M,Lowe R,Maleszka J,Conn D,Maleszka R,Hurd PJ

    更新日期:2018-10-01 00:00:00

  • A biometrical genome search in rats reveals the multigenic basis of blood pressure variation.

    abstract::A genome-wide search for multiple loci influencing salt-loaded systolic blood pressure (NaSBP) variation among 188 F2 progeny from a cross between the Brown-Norway and spontaneously hypertensive rat strains was pursued in an effort to gain insight into the polygenic basis of blood pressure regulation. The results sugg...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.5.2.164

    authors: Schork NJ,Krieger JE,Trolliet MR,Franchini KG,Koike G,Krieger EM,Lander ES,Dzau VJ,Jacob HJ

    更新日期:1995-09-01 00:00:00

  • Impact of genomics on research in the rat.

    abstract::The need to translate genes to function has positioned the rat as an invaluable animal model for genomic research. The significant increase in genomic resources in recent years has had an immediate functional application in the rat. Many of the resources for translational research are already in place and are ready to...

    journal_title:Genome research

    pub_type: 杂志文章,评审

    doi:10.1101/gr.3744005

    authors: Lazar J,Moreno C,Jacob HJ,Kwitek AE

    更新日期:2005-12-01 00:00:00

  • A combinatorial partitioning method to identify multilocus genotypic partitions that predict quantitative trait variation.

    abstract::Recent advances in genome research have accelerated the process of locating candidate genes and the variable sites within them and have simplified the task of genotype measurement. The development of statistical and computational strategies to utilize information on hundreds -- soon thousands -- of variable loci to in...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.172901

    authors: Nelson MR,Kardia SL,Ferrell RE,Sing CF

    更新日期:2001-03-01 00:00:00

  • Patterns of meiotic recombination on the long arm of human chromosome 21.

    abstract::In this study we quantify the features of meiotic recombination on the long arm of human chromosome 21. We constructed a 67. 3-centimorgan (cM) high-resolution, comprehensive, and accurate genetic linkage map of chromosome 21q using 187 highly polymorphic markers covering almost the entire long arm; 46 loci, consistin...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.138100

    authors: Lynn A,Kashuk C,Petersen MB,Bailey JA,Cox DR,Antonarakis SE,Chakravarti A

    更新日期:2000-09-01 00:00:00

  • A generic, cost-effective, and scalable cell lineage analysis platform.

    abstract::Advances in single-cell genomics enable commensurate improvements in methods for uncovering lineage relations among individual cells. Current sequencing-based methods for cell lineage analysis depend on low-resolution bulk analysis or rely on extensive single-cell sequencing, which is not scalable and could be biased ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.202903.115

    authors: Biezuner T,Spiro A,Raz O,Amir S,Milo L,Adar R,Chapal-Ilani N,Berman V,Fried Y,Ainbinder E,Cohen G,Barr HM,Halaban R,Shapiro E

    更新日期:2016-11-01 00:00:00

  • Random mutagenesis of proximal mouse chromosome 5 uncovers predominantly embryonic lethal mutations.

    abstract::A region-specific ENU mutagenesis screen was conducted to elucidate the functional content of proximal mouse Chr 5. We used the visibly marked, recessive, lethal inversion Rump White (Rw) as a balancer in a three-generation breeding scheme to identify recessive mutations within the approximately 50 megabases spanned b...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.3826505

    authors: Wilson L,Ching YH,Farias M,Hartford SA,Howell G,Shao H,Bucan M,Schimenti JC

    更新日期:2005-08-01 00:00:00