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You also agree to indemnify, defend, and hold harmless the Released Parties from any and all Claims in respect of the foregoing.
Calgary, Alberta T2E 5V8. Requests must be received no later than December 30, By checking that you have read the rules and regulations, You, the Sweepstakes entrant, have affirmatively reviewed, accepted, and agreed to all of the Official Rules above.
Un 1 seul prix par personne ou par foyer. Header Image. Contest Description. Entry Form. If you are randomly selected to win a shopping spree, which local participating store would you like to shop at?
I have read and agree to the terms below. Public votes will be collected, and the top three from each category will be assessed by a panel of judges.
One winner from each category, plus an overall grand prize winner, will be selected from these top-ranked photos. All decisions are final. Higher resolution photos are at an advantage—optimal resolution is dpi.
Photos are best if they can be reproduced to a width of 9 by 11 inches, or approximately x pixels. Judges may exclude entries that do not meet the above criteria, and are not able to provide individual feedback on submissions.
Winners will be notified by email. Prizes Judge's Tips Official Rules. Header Text. Lens us your pics! Help spotlight the unique beauty of the Teanaway Community Forest!
With six areas of focus, share stunning vistas, rivers, rock formations, wildlife, and community enthusiasm. Prizes will be awarded to winners in each category, with a grand prize selected overall.
Enter and vote today! How to text. One entry per category allowed. Judges will select the three highest-ranked finalists in each category.
Teanaway at Play. Teanaway at Play link. Flora and Fauna. Flora and Fauna link. Waterways link. Geology link. Macro Link. Youth Photography.
Youth Photography link. Teanaway at Play How do you play in the Teanaway? Category 1 Form. Awards management software for leading awards organisers to manage entry and judging online.
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ShortStack Reviews. Ease of Use. Customer Service. ShortStack makes contesting easy and engaging. An optional second column can contain names of the loci.
Any other columns will be ignored. Also, lines starting with will be ignored. Options --locus and --locifile are mutually exclusive. Also, if either is used, no de- novo cluster finding occurs.
The major methods are described below: Read-group-specific counts Quantification occurs separately for each read-group in the alignment.
The results are in the 'Counts. When there are multiple read-groups, this is helpful to gather the raw data for differential expression analysis.
There is always a read-group called 'main', which is all read-groups combined. All other loci are given a strand of. Note that the predominant RNA size need not be a majority..
It therefore probably allows some degree of false negatives e. If a locus fails a certain step, it is removed from consideration and given a specific code indicate what step it failed.
The codes are below in step-wise order. Increasing this size may allow you to find more MIRNAs, but will also slow down the runtime of the process.
N3: Major RNA abundance was less than 2 reads. N General failure to compute miRNA-star position if occurs, possible bug? N Maybe.
Y: Yes. Can support a de novo annotation of a new miRNA family. MIRNA analysis can be disabled with the --nohp option. This may save significant analysis time.
As of ShortStack version 3. Phasing Phasing here refers to a signature of periodicity of small RNA abundance that reflects dsRNA processing from a defined terminus.
For valid loci, ShortStack 3. ShortStack calculates the phase score in a 21 nt phase size for loci with a DicerCall of 21, or in a 24 nt phase size for loci with a DicerCall of 24, and returns the score.
Higher phasing scores indicate more phasing signature. Phase scores range from very near 0 worst up. The modification of the Guo et al.
Not all loci are subject to phasing analysis. These are assigned a PhaseScore of Log file A log of the run messages is created and written to Log.
ErrorLogs For debugging. Most users won't need to look at this. It stores the verbose outputs of bowtie-build, bowtie, samtools sort, and samtools merge commands that are not kep in the main Log.
Sometimes these are helpful in diagnosing bugs, particularly samtools sort and merge bugs due to memory issues. Stitched genome file If the input genome was 'stitched' see above , the stitched genome file will be put in the ShortStack outdir, along with its fai index temporarily during the run.
Both files will be deleted at the end of the run so you won't see them unless your run was killed before completion for some reason. Results file The file Results.
The columns are labeled in the first row, and are: 1. Locus: Coordinates of the locus in format Chr:Start-Stop 2.
Name: Name of the locus 3. Length: Length of the locus nts 4. Reads: Total number of primary alignments in the locus 5. RPM: Total number of primary alignments normalized to reads per million.
Note the the normalization factor includes all primary alignments.. UniqueReads: Number of uniquely aligned primary alignments in locus. FracTop: Fraction of primary alignments aligned to the top genomic strand 8.
Strand: Strand call for the locus 9. In cases of tie, MajorRNA is arbitrarily chosen from the tied entries. Lower numbers indicate loci that are more dominated by a single highly abundant RNA.
Can also be NA if the locus had no aligned reads. See above for full description of codes. PhaseScore: Phasing score for a phase size of 21 or 24nts according to a modified version of equation 3 of Guo et al doi: If the locus had a DicerCall of 21, phase score is for a 21 nt phasing register.
If the locus had a DicerCall of 24, the phase score is for a 24 nt phasing register. See above for full description of phasing analysis.
Short: Number of primary alignments that were shorter than --dicermin Long: Number of primary alignments that were longer than --dicermax end: Number of primary alignments of the indicated RNA size.
Unplaced file The Unplaced. This file is only created in a de-novo run. Columns show the sequence, its length, the total number of reads, the reads per million RPM and the number of equally valid genome alignments.
In some cases the number of genome alignments may not be able to be found. An entry of '? An entry of '?? Counts file The Counts.
For each locus, it shows the total raw read counts. Each read-group is broken out seperately, and the sum of all read groups is also shown termed 'main'.
Data from unplaced small RNAs, if present, are also included in Counts.OFFICIAL RULES. An official entry form must be completed for each photograph submitted. Photographers may submit one photo in each category for a TOTAL OF FIVE PHOTOS ONLY per photographer (six if the photographer is below the age of 18, and therefore able to participate in the Youth Photography category). 3/21/ · ShortStack calculates the phase score in a 21 nt phase size for loci with a DicerCall of 21, or in a 24 nt phase size for loci with a DicerCall of 24, and returns the score. Higher phasing scores indicate more phasing signature. Phase scores range from very near 0 (worst) up. For the safety of our staff and customers amidst COVID, we’ve had to adapt quickly and mindfully. Until further notice, our dining room is closed to customers and we are offering curbside pickup and delivery only, seven days a week. Our team of experts can help you plan your next marketing campaign, plus Shortstack and build it for you. Our styling features make meeting brand Werder Brem a breeze. Videos must Www.Mybet.Com entirely original in content. As you probably know, ShortStack our platform Neu.De Login Funktioniert Nicht marketers to run online contests, create unique landing pages and send emails.