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      Venus flytrap carnivorous lifestyle builds on herbivore defense strategies

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          Abstract

          Although the concept of botanical carnivory has been known since Darwin's time, the molecular mechanisms that allow animal feeding remain unknown, primarily due to a complete lack of genomic information. Here, we show that the transcriptomic landscape of the Dionaea trap is dramatically shifted toward signal transduction and nutrient transport upon insect feeding, with touch hormone signaling and protein secretion prevailing. At the same time, a massive induction of general defense responses is accompanied by the repression of cell death–related genes/processes. We hypothesize that the carnivory syndrome of Dionaea evolved by exaptation of ancient defense pathways, replacing cell death with nutrient acquisition.

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          RSEM: accurate transcript quantification from RNA-Seq data with or without a reference genome

          Background RNA-Seq is revolutionizing the way transcript abundances are measured. A key challenge in transcript quantification from RNA-Seq data is the handling of reads that map to multiple genes or isoforms. This issue is particularly important for quantification with de novo transcriptome assemblies in the absence of sequenced genomes, as it is difficult to determine which transcripts are isoforms of the same gene. A second significant issue is the design of RNA-Seq experiments, in terms of the number of reads, read length, and whether reads come from one or both ends of cDNA fragments. Results We present RSEM, an user-friendly software package for quantifying gene and isoform abundances from single-end or paired-end RNA-Seq data. RSEM outputs abundance estimates, 95% credibility intervals, and visualization files and can also simulate RNA-Seq data. In contrast to other existing tools, the software does not require a reference genome. Thus, in combination with a de novo transcriptome assembler, RSEM enables accurate transcript quantification for species without sequenced genomes. On simulated and real data sets, RSEM has superior or comparable performance to quantification methods that rely on a reference genome. Taking advantage of RSEM's ability to effectively use ambiguously-mapping reads, we show that accurate gene-level abundance estimates are best obtained with large numbers of short single-end reads. On the other hand, estimates of the relative frequencies of isoforms within single genes may be improved through the use of paired-end reads, depending on the number of possible splice forms for each gene. Conclusions RSEM is an accurate and user-friendly software tool for quantifying transcript abundances from RNA-Seq data. As it does not rely on the existence of a reference genome, it is particularly useful for quantification with de novo transcriptome assemblies. In addition, RSEM has enabled valuable guidance for cost-efficient design of quantification experiments with RNA-Seq, which is currently relatively expensive.
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            BLAST+: architecture and applications

            Background Sequence similarity searching is a very important bioinformatics task. While Basic Local Alignment Search Tool (BLAST) outperforms exact methods through its use of heuristics, the speed of the current BLAST software is suboptimal for very long queries or database sequences. There are also some shortcomings in the user-interface of the current command-line applications. Results We describe features and improvements of rewritten BLAST software and introduce new command-line applications. Long query sequences are broken into chunks for processing, in some cases leading to dramatically shorter run times. For long database sequences, it is possible to retrieve only the relevant parts of the sequence, reducing CPU time and memory usage for searches of short queries against databases of contigs or chromosomes. The program can now retrieve masking information for database sequences from the BLAST databases. A new modular software library can now access subject sequence data from arbitrary data sources. We introduce several new features, including strategy files that allow a user to save and reuse their favorite set of options. The strategy files can be uploaded to and downloaded from the NCBI BLAST web site. Conclusion The new BLAST command-line applications, compared to the current BLAST tools, demonstrate substantial speed improvements for long queries as well as chromosome length database sequences. We have also improved the user interface of the command-line applications.
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              BUSCO: assessing genome assembly and annotation completeness with single-copy orthologs.

              Genomics has revolutionized biological research, but quality assessment of the resulting assembled sequences is complicated and remains mostly limited to technical measures like N50.
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                Author and article information

                Journal
                Genome Res
                Genome Res
                genome
                genome
                GENOME
                Genome Research
                Cold Spring Harbor Laboratory Press
                1088-9051
                1549-5469
                June 2016
                June 2016
                : 26
                : 6
                : 812-825
                Affiliations
                [1 ]Center for Computational and Theoretical Biology, Campus Hubland Nord; Department of Bioinformatics, Biocenter, Am Hubland, University of Würzburg, D-97218 Würzburg, Germany;
                [2 ]Institute for Molecular Plant Physiology and Biophysics, Biocenter, University of Würzburg, 97082 Würzburg, Germany;
                [3 ]Department of Plant Systems Biology, University of Hohenheim, 70593 Stuttgart, Germany;
                [4 ]Department of Animal Ecology and Tropical Biology, Biocenter, Am Hubland, 97074 Würzburg, Germany;
                [5 ]Zoology Department, College of Science, King Saud University, Riyadh 11451, Saudi Arabia;
                [6 ]Bioorganic Chemistry Department, Max-Planck-Institute for Chemical Ecology, 07745 Jena, Germany;
                [7 ]Institute of Plant Biochemistry, Cluster of Excellence on Plant Sciences (CEPLAS), Heinrich-Heine-University, 40225 Düsseldorf, Germany
                Author notes
                [8]

                Present address: Max-Planck-Institute for Developmental Biology, Department of Molecular Biology, 72076 Tübingen, Germany

                Author information
                http://orcid.org/0000-0001-6557-4898
                http://orcid.org/0000-0003-3224-1362
                Article
                9509184
                10.1101/gr.202200.115
                4889972
                27197216
                09358963-789c-46df-87c4-a18d941d5e0b
                © 2016 Bemm et al.; Published by Cold Spring Harbor Laboratory Press

                This article, published in Genome Research, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 20 November 2015
                : 7 April 2016
                Page count
                Pages: 14
                Funding
                Funded by: European Research Council http://dx.doi.org/10.13039/501100000781
                Award ID: FP/20010-2015
                Award ID: 250194
                Funded by: King Saud University http://dx.doi.org/10.13039/501100002383
                Award ID: IRG14-08
                Categories
                Research

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