Searching journal content for articles similar to Gansauge and Meyer 24 (9): 1543.

Displaying results 1-10 of 68
For checked items
  1. ...prehistory. Nat Commun 5: 5257. doi:10.1038/ncomms6257 ↵Gansauge M-T, Meyer M. 2013. Single-stranded DNA library preparation for the sequencing of ancient or damaged DNA. Nat Protoc 8: 737–748. doi:10.1038/nprot.2013.038 ↵Gansauge M-T, Meyer M. 2019. A method for single-stranded ancient DNA library...
  2. ...oligonucleotides that are free in solution as baits to fish out complementary sequences in a DNA library (Gnirke et al. 2009) has been transformative for studying ancient DNA. Under appropriate chemical and temperature conditions, these baits hybridize to targeted molecules so other molecules can be washed away...
  3. ...extract using UDG-treatment methods, as described in Rohland et al. (2015) and Gansauge et al. (2020), respectively. These methods remove ancient DNA damage at the interior of each DNA sequence, while preserving characteristic ancient DNA damage at the terminal ends of the molecules, to be used...
  4. ...DNA recovered and frequency of damage at the terminal nucleotide of the DNA molecule (a commonly used measure of ancient DNA authenticity). Based on these results, we selected an additional 16 archaeological samples for further study from a wide range of geographic locations with varying climates...
  5. ...apoptosis in the trophoblast surrounding the fetus (Tjoa et al. 2006).Beyond the identification of genetic variants, the sequencing of billions of DNA fragments has allowed inferences about the structures of molecules and characteristics of DNA damage that have proven critical for the development of new...
  6. ...and methylation information cannot be directly obtained from short-read sequencing because amplification of the original DNA molecule is necessary for clustering. We and others have therefore used the redundancy of the double-stranded DNA to identify DNA methylation information and genomic variants simultaneously...
  7. ...is a bias against >5-kbp-long transcripts, probably owing to incomplete reverse transcription. To overcome this limitation, size-selection of cDNAs before sequencing could be a potential solution. This has been successfully shown to sequence a 106-kbp-long transcript from the mouse Ttn gene (Uapinyoying et...
  8. ...in library preparation. The efficiency of library preparation is determined by comparing the number of oligonucleotide library molecules generated in the sample libraries to those in extraction and library blanks. Sequencing the shortest ancient DNA fragments Genome Research 1233 www..org preserved...
  9. ...represents the anti-reference strand. (B) Size selection using 0.5× SPRI beads. Uncut, genomic DNA binds to the beads and allows the recovery of the homogenously sized excised fragments in solution. (C) Double-stranded DNA molecule fragmented and ligated with double-stranded DS adapters. Adapters contain 10...
  10. ...sequencing depth. The percentage of IESs involved in at least one IES–IES junction is indicated above the barplot.Genome-wide detection of transient IES–IES junctionsWe took advantage of the purity of FANS-sorted anlagen to increase our ability to detect transient DNA molecules produced during IES excision...
For checked items

Preprint Server