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      Identification of QTLs and Meta‐QTLs for Seven Agronomic Traits in Multiple Maize Populations under Well‐Watered and Water‐Stressed Conditions

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          Exploration, normalization, and summaries of high density oligonucleotide array probe level data.

          In this paper we report exploratory analyses of high-density oligonucleotide array data from the Affymetrix GeneChip system with the objective of improving upon currently used measures of gene expression. Our analyses make use of three data sets: a small experimental study consisting of five MGU74A mouse GeneChip arrays, part of the data from an extensive spike-in study conducted by Gene Logic and Wyeth's Genetics Institute involving 95 HG-U95A human GeneChip arrays; and part of a dilution study conducted by Gene Logic involving 75 HG-U95A GeneChip arrays. We display some familiar features of the perfect match and mismatch probe (PM and MM) values of these data, and examine the variance-mean relationship with probe-level data from probes believed to be defective, and so delivering noise only. We explain why we need to normalize the arrays to one another using probe level intensities. We then examine the behavior of the PM and MM using spike-in data and assess three commonly used summary measures: Affymetrix's (i) average difference (AvDiff) and (ii) MAS 5.0 signal, and (iii) the Li and Wong multiplicative model-based expression index (MBEI). The exploratory data analyses of the probe level data motivate a new summary measure that is a robust multi-array average (RMA) of background-adjusted, normalized, and log-transformed PM values. We evaluate the four expression summary measures using the dilution study data, assessing their behavior in terms of bias, variance and (for MBEI and RMA) model fit. Finally, we evaluate the algorithms in terms of their ability to detect known levels of differential expression using the spike-in data. We conclude that there is no obvious downside to using RMA and attaching a standard error (SE) to this quantity using a linear model which removes probe-specific affinities.
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            Improved maize reference genome with single-molecule technologies

            An improved reference genome for maize, using single-molecule sequencing and high-resolution optical mapping, enables characterization of structural variation and repetitive regions, and identifies lineage expansions of transposable elements that are unique to maize. Supplementary information The online version of this article (doi:10.1038/nature22971) contains supplementary material, which is available to authorized users.
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              Ribosomal DNA spacer-length polymorphisms in barley: mendelian inheritance, chromosomal location, and population dynamics.

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                Author and article information

                Journal
                Crop Science
                Crop Sci.
                Wiley
                0011-183X
                1435-0653
                March 2018
                March 2018
                March 2018
                : 58
                : 2
                : 507-520
                Affiliations
                [1 ]Gansu Key Laboratory of Crop Improvement and Germplasm Enhancement Lanzhou 730070 China
                [2 ]Gansu Provincial Key Laboratory of Aridland Crop Science Lanzhou 730070 China
                [3 ]College of Agronomy Gansu Agricultural Univ. Lanzhou 730070 China
                Article
                10.2135/cropsci2016.12.0991
                2d2e60d4-5079-4f50-9ff3-7a36266cbd39
                © 2018

                http://creativecommons.org/licenses/by-nc-nd/4.0/

                http://doi.wiley.com/10.1002/tdm_license_1.1

                History

                Quantitative & Systems biology,Biophysics
                Quantitative & Systems biology, Biophysics

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