To assess the reliability of our regulon mapping, we collected microarray data of PCC6803 under hyperosmotic stress from the public domain (see Additional file 8).
Using an alternative mapping criterion, we collected the sequences of the 3' end modified fragments by analyzing their relative abundances in all modification events.
In order to close this gap on the genetic map of Southeast Asia, we collected DNA samples from 327 unrelated donors originating from 13 of the 14 political regions representing the most important ethnic groups of Myanmar and genotyped the entire mitochondrial control region (16024 16569; 1–576) of all samples and the entire mitochondrial genome of a subset of 44 selected samples.
Before mapping the raw reads, we collected 1.4 million wheat ESTs from several databases, clustered into 127,039 Uniref clusters yielding to the best of our knowledge, the largest well-annotated EST databank in wheat (Additional file 1: Method S2).
After mapping and variant calling we collected for each combination of coverage and variant allele frequencies the number of false positives (FP), true positives (TP), false negatives (FN), and true negatives (TN).
In order to enlarge coverage of the interaction maps, we also collected physical interactions for Caenorhabditis elegans (worm) and Saccharomyces cerevisiae (yeast).
In contrast to earlier studies employing the same task, we collected multiple maps for each subject as a function of starting gaze position.
To test this hypothesis, we collected cognitive maps of northern pike (Esox lucius) ecology from anglers (N=235) and assessed their relation to anglers' level of specialization and preferred target species.
All the sequence data we collected were mapped onto the human genome and clustered.
DOI: http://dx.doi.org/10.7554/eLife.02481.009 Since negative stain EM of ClpB (BAP) in complex with ClpP gave a clear result different from all previous cryo EM maps of ClpB and Hsp104, we collected cryo EM data on BAP-ClpP as well as on ClpB alone.
