Searching journal content for articles similar to Lunter and Goodson 21 (6): 936.

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  1. ...immediately Table 1. Quality statistics for 1-mg Illumina and 10-pg-level tagmented libraries Target DNA E. coli gDNA Method Illumina Tagmentation AcuI BsgI/BpmI Blended from all four DNA input 1 mg 10 pg 23 10 pg 43 10 pg Demultiplexed reads >phred 20 3,932,654 (100%) 4,125,988 (100%) 4,684,314 (100%) 3...
  2. ...indel model for Illumina reads and were not designed for analyzing pools of samples. To the best of our knowledge, our method is the first to address the realignment problem and various sources of errors explicitly in a single statistical framework, in particular the modeling of context...
  3. ...is lower at approximately fourfold (Orangutan Genome Sequencing Consortium, in prep.). We were able to take advantage of a data set of short reads at approximately 10-fold statistical coverage from a single Bornean orangutan (Pongo pygmaeus pygmaeus) thatwas shotgun-sequenced using the Illumina short read...
  4. .... The sequencing was done with Illumina HiSeq 2000 or NovaSeq 6000 by the NGS platform of the University of Bern. Raw reads of all individuals (Fig. 1A; Supplemental Table S1) were mapped to the reference of M. arvalis (BioProject ID: PRJNA737461; A Gouy, X Wang, A Kapopoulou, et al., in prep.) using Stampy 1...
  5. ...Indian state of Himachal Pradesh (Halligan et al. 2010, 2013). Reads were mapped against mouse mm9 using BWA (Li and Durbin 2009) and Stampy (Lunter and Goodson 2011). As coding regions in mm9 are well annotated, use of more recent builds would not affect our conclusions. Duplicate reads were marked...
  6. ...M. 2011. Stampy: a statistical algorithm for sensitive and fast mapping of Illumina sequence reads. Genome Res 21: 936–939. ↵Lynch M. 2007. The origins of architecture. Sinauer Associates, Inc., Sunderland, MA. ↵MacCallum I, Przybylski D, Gnerre S, Burton J, Shlyakhter I, Gnirke A, Malek J, Mc...
  7. .... This has previously been investigated by sequencing autosomal and mitochondrial DNA (mtDNA), but large-scale sequence analysis of the male-specific region of the Y Chromosome (MSY) has not yet been undertaken. Here, we use the human MSY reference sequence as a basis for sequence capture and read mapping...
  8. ...), and the mapping was further improved with Stampy (version 1.0.20) (Lunter and Goodson 2011). PCR duplicates were removed by “rmdup” in SAMtools (version 0.17) (Li et al. 2009). We realigned reads at gapped regions with GATK (version 2.6) (DePristo et al. 2011). Population structure, phylogeny, network, and Tree...
  9. ...prefrontal cortices (Lonsdale et al. 2013), and 531 samples from diverse human and mouse tissues (Merkin et al. 2012; Lonsdale et al. 2013); Illumina Human BodyMap Project (European Nucleotide Archive [ENA; http://www.ebi.ac.uk/ena/]; accession number ERA022994) to show that thousands of micro...
  10. ...to the manufacturer’s protocol (Illumina Inc.). These were shotgun sequenced on either Illumina’s Genome Analyzer IIx system or Illumina’s HiSeq 2000 system, according to the manufacturer’s protocol (Illumina Inc.). Quality-filtered, paired-end sequence reads were mapped to the H. melpomene scaffolds (version 1...
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