<style face="normal" font="default" size="100%">A new parallel pipeline for DNA methylation analysis of long reads datasets.</style>

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<style face="normal" font="default" size="100%">A new parallel pipeline for DNA methylation analysis of long reads datasets.</style>

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<style face="normal" font="default" size="100%">267 Spanish exomes reveal population-specific differences in disease-related genetic variation.</style>

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<style face="normal" font="default" size="100%">Assessment of Targeted Next-Generation Sequencing as a Tool for the Diagnosis of Charcot-Marie-Tooth Disease and Hereditary Motor Neuropathy.</style>

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<style face="normal" font="default" size="100%">HPG pore: an efficient and scalable framework for nanopore sequencing data.</style>

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<style face="normal" font="default" size="100%">Assessing the impact of mutations found in next generation sequencing data over human signaling pathways.</style>

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<style face="normal" font="default" size="100%">Babelomics 5.0: functional interpretation for new generations of genomic data.</style>

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<style face="normal" font="default" size="100%">Combining tumor genome simulation with crowdsourcing to benchmark somatic single-nucleotide-variant detection.</style>

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<style face="normal" font="default" size="100%">Concurrent and Accurate Short Read Mapping on Multicore Processors.</style>

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<style face="normal" font="default" size="100%">Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease.</style>

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<style face="normal" font="default" size="100%">A Parallel and Sensitive Software Tool for Methylation Analysis on Multicore Platforms.</style>

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<style face="normal" font="default" size="100%">Acceleration of short and long DNA read mapping without loss of accuracy using suffix array.</style>

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<style face="normal" font="default" size="100%">A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium.</style>

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<style face="normal" font="default" size="100%">A New Overgrowth Syndrome is Due to Mutations in RNF125.</style>

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<style face="normal" font="default" size="100%">Genome Maps, a new generation genome browser.</style>

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<style face="normal" font="default" size="100%">A map of human microRNA variation uncovers unexpectedly high levels of variability.</style>

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<style face="normal" font="default" size="100%">Qualimap: evaluating next-generation sequencing alignment data.</style>

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<style face="normal" font="default" size="100%">Using GPUs for the Exact Alignment of Short-read Genetic Sequences by Means of the Burrows–Wheeler Transform.</style>

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<style face="normal" font="default" size="100%">Initial genomics of the human nucleolus.</style>