Simulations with time-dependent mineral surface areas show a sequence of solid alteration products, described by: magnetite → cronstedtite → berthierine → chlorite.
This technique has been shown to be a powerful approach for establishing the sequence of solid phases produced during crystallization [21, 22, 23] and for the discovery of new (transient) solid forms [24].
Indeed, recent work in a related domain, large-scale sequencing of solid tumors, demonstrates the statistical challenges in attempting to make this distinction [52], [53], [54], [55], [56], [57].
This in-situ NMR technique has been shown to be a powerful strategy for establishing the sequence of solid phases produced during crystallization 3 (inter alia, indicating the time-window during which each transient phase is present) and for the discovery of new polymorphs.
They also emphasize the need for a better clinical understanding of the time sequence of solid-tumour recovery in relation to the time sequence of marrow recovery.
Motif patterns consisting of sequences of intermixed solid and don't-care characters have been introduced and studied in connection with pattern discovery problems of computational biology and other domains.
The resulting cDNA libraries consisted entirely of random length fragments representing the 5′ end of an mRNA molecule with the full SOLiD P1 adaptor and the internal adaptor sequence of the SOLiD P2 adaptor.
The observed precipitation sequence of "supersaturated solid solution → NiAl → NiAl + Cu" is substantially different from the one previously reported in Cu-strengthened steels, which involves the process of "supersaturated solid solution → Cu → Cu + NiAl".
cDNA were produced by RT PCR with Superscript III (Invitrogen) and a random primer consisting of the internal adaptor sequence of the SOLiD P2 adaptor with a 5′ hexomeric degenerate sequence (5′-CTGCCCCGGGTTCCTCATTCTCTNNNNNC-3′).
