PRIDE PROXI spectra returning mzs not in order #73
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Fetching a spectrum from PRIDE via PROXI such as:
http://wwwdev.ebi.ac.uk/pride/proxi/archive/v0.1/spectra?resultType=full&usi=mzspec:PXD000966:CPTAC_CompRef_00_iTRAQ_12_5Feb12_Cougar_11-10-11.mzML:scan:11850:[UNIMOD:214]YYWGGLYSWDMSK[UNIMOD:214]/2
returns the mzs in random order. This is not against the current spec, which does not specify. But it is breaking the Lorikeet viewer at ProteomeCentral. Seems like many applications may assume mzs in order.
What should be the resolution?
Does the random order of mzs at PRIDE match the same order of intensities? One risk of separate arrays is that they become unaligned.
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