Nebula Genomics Whole Genome Sequencing 30x — Reviews & Rating - Prooffeed
Prooffeed Nebula Genomics Nebula Genomics Whole Genome Sequencing 30x

Nebula Genomics Whole Genome Sequencing 30x

Brand: Nebula Genomics

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Nebula Genomics grew out of George Church's lab at Harvard and sells sequencing, not a marker chip. The 30x kit reads close to all of the genome, tens of gigabytes of data that can be downloaded and kept, instead of the few hundred thousand markers a standard ancestry test looks at. Deep ancestry reporting covers maternal and paternal haplogroups plus comparison with ancient populations.

For a researcher who plans to feed raw data into third party tools, this is the one kit that never needs repeating. The price is several times a chip test, the lab takes longer than a swab kit, and there is no crowded cousin matching network inside Nebula. Registration can stay anonymous and reports are refreshed as new papers appear, which is unusual in this market.

Pros

  • Full 30x genome, not a marker chip
  • Raw data download you can reuse
  • Haplogroups and ancient ancestry reports
  • Anonymous sign up possible
  • Reports refreshed with new research

Cons

  • Costs several times a chip test
  • No large relative matching pool
  • Longer laboratory turnaround
  • Big files need extra tools to read

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