4.8 Article

iFISH is a publically available resource enabling versatile DNA FISH to study genome architecture

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NATURE COMMUNICATIONS
卷 10, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-019-09616-w

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资金

  1. Sony Imaging Products & Solutions, Inc.
  2. Swedish Research Council [2013-32485-100360-69, 521-2014-2866, 621-2014-5503]
  3. Knut and Alice Wallenberg Foundation [2016.0121, 2015.0096]
  4. Ming Wai Lau Centre for Reparative Medicine [2-343/2016]
  5. CIMED [2-388/2016-40]
  6. Ragnar Soderberg Foundation [M67/13]
  7. Swedish Cancer Research Foundation [CAN 2015/585]
  8. Ragnar Soderberg Foundation
  9. Science for Life Laboratory
  10. Karolinska Institutet KID Funding Program
  11. Human Frontier Science Program (HFSP Career Development Award)
  12. European Research Council [StG-2016_GENOMIS_715727]
  13. Svenska Sallskapet for Medicinsk Forskning (SSMF)

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DNA fluorescence in situ hybridization (DNA FISH) is a powerful method to study chromosomal organization in single cells. At present, there is a lack of free resources of DNA FISH probes and probe design tools which can be readily applied. Here, we describe iFISH, an open-source repository currently comprising 380 DNA FISH probes targeting multiple loci on the human autosomes and chromosome X, as well as a genome-wide database of optimally designed oligonucleotides and a freely accessible web interface (http://ifish4u.org) that can be used to design DNA FISH probes. We individually validate 153 probes and take advantage of our probe repository to quantify the extent of intermingling between multiple heterologous chromosome pairs, showing a much higher extent of intermingling in human embryonic stem cells compared to fibroblasts. In conclusion, iFISH is a versatile and expandable resource, which can greatly facilitate the use of DNA FISH in research and diagnostics.

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