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Submit digital photos in JPEG format only. Higher resolution photos dpi, 9 x 11 inches or approximately x pixels are preferable.
How do you play in the Teanaway? Show us people enjoying the outdoors, be it at a campsite, hiking a trail, on horseback, by snowmobile or in the water.
Photographers must have permission from any person portrayed in the photo, and all activities depicted must comply with Leave No Trace.
Visitors can find myriad species in the Teanaway, from elk to white headed woodpeckers, lupine to balsamroot. Please give wildlife plenty of space and keep safety in mind when photographing living plants and animals.
The Teanaway contains nearly miles of free-flowing rivers and streams that beckon people and wildlife alike with cold, clear water. In fact, the Teanaway was conserved first and foremost for its values as high-elevation watershed!
Help us share that importance by photographing these rushing rivers. They tell a fascinating story about the forces that helped shape our region — now we ask you to help them share it.
The Teanaway's a favorite spot with families, and a great place to introduce kids to the outdoors. If you're under 18 and enjoy exploring the Teanaway with your camera, we want to see through your eyes.
Submit here for a chance to win! The Teanaway is full of hidden worlds - insects, fungi, pebbles, and infinitely unique organic patterns.
What can you find when you get up close and personal? Your participation in the Teanaway Photo Contest helps us encourage exploration and preservation of Washington's first Community Forest.
As thanks, we've put together some great prize packages! The Scott Seymour Prize In honor of Scott Seymour, our judges will select one overall grand prize winner, who will receive:.
Scott was an avid photographer and lover of the Teanaway, who shared his perspective on Upper Kittitas County with the community for years.
His optimism and eye for beauty brightened many days. With permission from his family, we hope to encourage others to do the same.
These five first place winners will receive:. Consider these handy tips for capturing a winning photo! Pictures are powerful, and we want to ensure that the photos we feature show hiking and camping practices that set good examples for Teanaway visitors.
As a general rule, our judges will only select a if it depicts hikers staying on the trail or durable surface like snow or rock and practicing good Leave No Trace principles.
Please keep dogs on leash for photos that are entered in the photo contest. Tents should be placed on a durable surface and camps should be Leave No Trace compliant.
This is faster than u and f, but performs much more poorly at properly placing multi-mapped reads. Achieves high sensitivity, but very low precision.
Very fast, but ignores large quantities of data. Achieves high precision, but very low sensitivity. The default setting for --mmap is u ranmax When running mmap method u or f, there are some cases where no guidance can be given, and so the choice on where to put a multi-mapped read is still random.
In those cases, the option ranmax will suppress any alignment where the choice is 'too' random. By default, --ranmax is set at 3, so that if a read can't be placed confidently, no placement is done if there are more than 3 choices.
Alignment output format Final alignments are sorted bam or cram formatted alignments. XX:i tags: Added by ShortStack to each line, this indicates the total number of valid alignments found for the read.
XZ:f tags: Added by ShortStack to each line, this indicates the calculated probability of placement for the read. Any properly formatted bam or cram file should work with ShortStack, subject to the requirements below.
However, for best performance, it is recommended to use ShortStack for alignments as well. Requirements for input bam or cram files: 1.
Header must be present, and contain SQ lines. File most be sorted. Read groups will not be recognized unless they are properly noted in the header.
Paired-end, spliced, clipped, padded, or gapped alignments will be ignored, with a warning to the user.
Reads marked as secondary alignments bit set in the FLAG will not be used. The mincov threshold can also be specified in terms of reads per million by using a value such as 3.
Using a rpm threshold allows the sensitivity of cluster discovery to be normalized between libraries of different sizes. Alternatively, reads per million mapped rpmm can be specified: A --mincov of 1.
Only small RNAs with an abundance higher than the limit set by option --mincov are reported. These small RNAs typically inlcude RNAs that could not be aligned anywhere on the reference, as well as multi-mapped RNAs where ShortStack did not choose a alignment position for see alignment methods.
For just one or a few loci, the option --locus can be used. The argument should be a coordinate in the format Chr:Start-Stop. Multiple loci can be specified in option --locus by using commas to delimit them.
For larger lists of user-defined loci, and external file can be used instead, specified with option --locifile. The file is a plain-text , tab-delimited format.
The first column should list the coordinates in Chr:Start-Stop format. 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. This sweepstakes is void where prohibited by law and is subject to all applicable federal and municipal laws.
If the selected entrant cannot be contacted within fourteen 14 days of selection or there is a return of any prior notification as undeliverable, that entrant will be disqualified and an alternate entrant will be selected from among the remaining eligible entries.
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The Sponsor s and the independent Sweepstakes organization are not responsible for: i late- received, illegible, incomplete, falsified, destroyed, unintelligible, incomplete, lost, irretrievable or misdirected entries and all such entries are void ii entries which fail to comply with these Sweepstakes Rules.
All entries become the permanent property of the Sponsor s and none will be returned. This Sweepstakes is void where prohibited by law and is subject to all applicable federal, provincial and municipal laws.
The Sponsor s respects your right to privacy. This Promotion is in no way sponsored, endorsed or administered by, or associated with Facebook or any represented prize image brands or manufacturers.
On 3 February , Short Stack announced via their Facebook page that they had reunited for a second time.
It was revealed soon after that to celebrate the reunion they would be going on their first tour in four years. Short Stack have toured several times, to promote each of their albums, and often held meet and greets.
In , they opened for The Vamps in their Australian tour but they were later asked to leave the tour by the Vamps management. From Wikipedia, the free encyclopedia.
Short Stack. Release date: 21 August First album following reformation. Australia: Sunday Morning Records. XYZ Networks. Retrieved 19 November Retrieved 31 March Central Coast Express Advocate.
Retrieved 30 September Retrieved 29 July TV Tonight. Retrieved 20 December Retrieved 30 October Take Archived from the original on 5 October Retrieved 5 October The Music Network.
Retrieved 12 August Retrieved 24 August Australian Broadcasting Corporation. Retrieved 18 March May September MTV Australia. Nova FM. Channel 5.