8 research outputs found
Additional file 3: Table S1. of Transcriptome analysis of smooth cordgrass (Spartina alterniflora Loisel), a monocot halophyte, reveals candidate genes involved in its adaptation to salinity
Protein families found in Spartina alterniflora unigenes retrieved from Pfam database. (XLSX 229 kb
Additional file 2: Figure S1. of Transcriptome analysis of smooth cordgrass (Spartina alterniflora Loisel), a monocot halophyte, reveals candidate genes involved in its adaptation to salinity
Percentage distribution of GC content between Spartina alterniflora and rice genes. Figure S2 Gene family distribution among the four monocots, Spartina alterniflora (Sa), Oryza sativa (Os), Sorghum bicolor (Sb) and Zea mays (Zm). The homologous genes from each monocot species were clustered to represent gene family. The number of homologous genes shared by different species is represented by gene families at intersection. Figure S3 Functional GO terms for gene families specific to Spartina alterniflora indicating coverage of different functional category genes specific to S. alterniflora. Figure S4 A histogram showing the GC content distribution in different sets of genes of Spartina alterniflora. NP, set of genes having similarity outside of poaceae; PS, poaceae specific genes; All, whole S. alterniflora transcriptome; and SS, S. alterniflora-specific genes. Figure S5 Distribution of different repeat unit size of the SSRs identified in Spartina alterniflora transcriptome. Figure S6 Distribution of different types of SSR motifs in Spartina alterniflora unigenes. Figure S7 Representative gel showing DNA profile of 13 (CP1 through CP13) Spartina alterniflora accessions produced by five SSR primers derived from the contigs. (PPTX 778 kb
Additional file 1: of Transcriptome analysis of smooth cordgrass (Spartina alterniflora Loisel), a monocot halophyte, reveals candidate genes involved in its adaptation to salinity
The comparative analysis among Spartina alterniflora reads with reads of Salterniflora [34] and unigenes of S. pectinata [78]. (XLSX 154 kb
Map of included health centers.
<p>The village of Atalaya (−3.58, −73.75), located 59 km to the West of Iquitos, is not displayed on the map.</p
Sensitivity, faint line intensity and cross-reactions of the different RDT products for detection of <i>P. falciparum</i> and <i>P. vivax</i>.
*<p>cross-reactions excluded.</p>†<p>only <i>P. vivax</i> samples were considered.</p
Patient data and parasite density of the final sample collection.
*<p>artesunate + mefloquine since 2 days (n = 1), chloroquine since 2 days (n = 2), full course of chloroquine/primaquine (n = 1) at least >1 week ago (exact date not known).</p
<i>P. falciparum</i> samples not detected by PfHRP2-detecting RDTs: <i>pfhrp2</i> and <i>pfhrp3</i> PCR results and PfHRP2 ELISA results.
<p>+ = positive, − = negative, +/− = weak positive.</p>*<p>This sample contained only gametocytes.</p
Harnessing C–H Borylation/Deborylation for Selective Deuteration, Synthesis of Boronate Esters, and Late Stage Functionalization
Ir-catalyzed deborylation
can be used to selectively deuterate
aromatic and heteroaromatic substrates. Combined with the selectivities
of Ir-catalyzed C–H borylations, uniquely labeled compounds
can be prepared. In addition, diborylation/deborylation reactions
provide monoborylated regioisomers that complement those prepared
by C–H borylation. Comparisons between Ir-catalyzed deborylations
and Pd-catalyzed deborylations of diborylated indoles described by
Movassaghi are made. The Ir-catalyzed process is more effective for
deborylating aromatics and is generally more effective in the monodeborylation
of diborylated thiophenes. These processes can be applied to complex
molecules such as clopidogrel