ReSeq-profiles

December 1, 2020 · View on GitHub

For best results it is always advised to create your own profiles from a dataset very closely matching the desired sequencer, chemistry, fragmentation, adapters, PCR cycles, etc. Furthermore, training on the same or a closely related species, is best to be sure that the necessary profile space (e.g. range of GC content) is well populated. However, in many situations there is no specific case that should be simulated, but a wide variety of datasets is important. Under this condition finding good datasets is tedious work and recreating the same profile from a given dataset does not help to ensure the quality of the simulated data. Therefore, this repository is designed to provide high-quality profiles with detailed information on the original datasets. Whenever possible, method benchmarks should be performed on the simulated and the original dataset to verify that the simulation created realistic conditions for the particular use case.

DatasetYearSequencerAdapterSpeciesRead lengthFragment lengthCoverageProfileIpf
SRR490124≤ 2013HiSeq 2000TruSeqE. coli100164449XX
BaseSpace, HiSeq 4000: Nextera XT (B.cereus, E.coli, R.sphaeroides), Ecoli1_L0012015HiSeq 4000NexteraE. coli151-508XX
BaseSpace, HiSeq 4000: Nextera XT (B.cereus, E.coli, R.sphaeroides), Bcereus1_L0012015HiSeq 4000NexteraB. cereus151-508XX
PRJEB33197 COLO829BL control samples2019NovaSeq 6000TruSeqH. sapiens151512131XX
DRR0580602016MiSeqTruSeqE. coli251231≥ 214XX

In case you created a profile that reflects a given dataset well, please contact me to share it with others.