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Mini Dragon Group (ages 6-7)

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Finder Windows 1.5.11


Want to help clients quickly find the nearest offline store with your products? The Magento Store Locator extension enables you to add addresses of physical retail stores to your website just in a few clicks. This Magento 1 store finder allows creating as many store locations as you need and displaying them on a separate page using Google maps. Give customers Magento 1 map with exact store locations to enhance their shopping experience. Also, you can provide customers with the advanced return/exchange system to enhance their shopping experience.




Finder Windows 1.5.11



Update vendored dependencies- attrs from 20.3.0 to 21.2.0- cerberus from 1.3.2 to 1.3.4- certifi from 2020.11.8 to 2021.5.30- chardet from 3.0.4 to 4.0.0- click from 7.1.2 to 8.0.1- distlib from 0.3.1 to 0.3.2- idna from 2.10 to 3.2- importlib-metadata from 2.0.0 to 4.6.1- importlib-resources from 3.3.0 to 5.2.0- jinja2 from 2.11.2 to 3.0.1- markupsafe from 1.1.1 to 2.0.1- more-itertools from 5.0.0 to 8.8.0- packaging from 20.8 to 21.0- pep517 from 0.9.1 to 0.11.0- pipdeptree from 1.0.0 to 2.0.0- ptyprocess from 0.6.0 to 0.7.0- python-dateutil from 2.8.1 to 2.8.2- python-dotenv from 0.15.0 to 0.19.0- pythonfinder from 1.2.5 to 1.2.8- requests from 2.25.0 to 2.26.0- shellingham from 1.3.2 to 1.4.0- six from 1.15.0 to 1.16.0- tomlkit from 0.7.0 to 0.7.2- urllib3 from 1.26.1 to 1.26.6- zipp from 1.2.0 to 3.5.0


Update vendored libraries:- scandir to 1.9.0- click-completion to 0.4.1- semver to 2.8.1- shellingham to 1.2.4- pytoml to 0.1.18- certifi to 2018.8.24- ptyprocess to 0.6.0- requirementslib to 1.1.5- pythonfinder to 1.0.2- pipdeptree to 0.13.0- python-dotenv to 0.9.1 #2639


When I run the command this is what I see$ pip install django==2.2.1DEPRECATION: Python 2.7 will reach the end of its life on January 1st, 2020. Please upgrade your Python as Python 2.7 won't be maintained after that date. A future version of pip will drop support for Python 2.7.Collecting django==2.2.1 ERROR: Could not find a version that satisfies the requirement django==2.2.1 (from versions: 1.1.3, 1.1.4, 1.2, 1.2.1, 1.2.2, 1.2.3, 1.2.4, 1.2.5, 1.2.6, 1.2.7, 1.3, 1.3.1, 1.3.2, 1.3.3, 1.3.4, 1.3.5, 1.3.6, 1.3.7, 1.4, 1.4.1, 1.4.2, 1.4.3, 1.4.4, 1.4.5, 1.4.6, 1.4.7, 1.4.8, 1.4.9, 1.4.10, 1.4.11, 1.4.12, 1.4.13, 1.4.14, 1.4.15, 1.4.16, 1.4.17, 1.4.18, 1.4.19, 1.4.20, 1.4.21, 1.4.22, 1.5, 1.5.1, 1.5.2, 1.5.3, 1.5.4, 1.5.5, 1.5.6, 1.5.7, 1.5.8, 1.5.9, 1.5.10, 1.5.11, 1.5.12, 1.6, 1.6.1, 1.6.2, 1.6.3, 1.6.4, 1.6.5, 1.6.6, 1.6.7, 1.6.8, 1.6.9, 1.6.10, 1.6.11, 1.7, 1.7.1, 1.7.2, 1.7.3, 1.7.4, 1.7.5, 1.7.6, 1.7.7, 1.7.8, 1.7.9, 1.7.10, 1.7.11, 1.8a1, 1.8b1, 1.8b2, 1.8rc1, 1.8, 1.8.1, 1.8.2, 1.8.3, 1.8.4, 1.8.5, 1.8.6, 1.8.7, 1.8.8, 1.8.9, 1.8.10, 1.8.11, 1.8.12, 1.8.13, 1.8.14, 1.8.15, 1.8.16, 1.8.17, 1.8.18, 1.8.19, 1.9a1, 1.9b1, 1.9rc1, 1.9rc2, 1.9, 1.9.1, 1.9.2, 1.9.3, 1.9.4, 1.9.5, 1.9.6, 1.9.7, 1.9.8, 1.9.9, 1.9.10, 1.9.11, 1.9.12, 1.9.13, 1.10a1, 1.10b1, 1.10rc1, 1.10, 1.10.1, 1.10.2, 1.10.3, 1.10.4, 1.10.5, 1.10.6, 1.10.7, 1.10.8, 1.11a1, 1.11b1, 1.11rc1, 1.11, 1.11.1, 1.11.2, 1.11.3, 1.11.4, 1.11.5, 1.11.6, 1.11.7, 1.11.8, 1.11.9, 1.11.10, 1.11.11, 1.11.12, 1.11.13, 1.11.14, 1.11.15, 1.11.16, 1.11.17, 1.11.18, 1.11.20)ERROR: No matching distribution found for django==2.2.1


When I click "ok" once, the "Add New Torrent" windows disappeared and I unable to click anywhere on uTorrent. Cannot quit, too. I have to "force quit" the program and restart to, so it will work properly again.


There are a bunch of ways to trigger the problem, all of which seem to involve more than one torrent being added. The simplest way to trigger the problem is to have a few torrent files, multiple select them in the finder and then open them. utorrent will present a single 'add torrrent' dialog window which can be added as expected and that's all. Any further attempt to use the user interface results in just a beep and no action. Force quit or kill from a shell are the only way out (quit from the menus and close window button also both fail to function with an error beep).


I updated the to the most recent version of uTorrent as well (Version 1.5.11 (25801) and also using latest version of Lion (10.7.2)) and now the feature where I can select and deselect files prior to actually downloading is enabled (thank you btw), but it completely destroys the interface itself. I cannot click on anything, select, minimize, close, or even quit; however, the torrent does continue to download. The only thing I can do is move the box around.


Since 1.5.11 SLF4J software preempts the inevitable stack overflow error by throwing an exception with details about the actual cause of the problem. This is deemed to be better than leaving the user wondering about the reasons of the StackOverflowError.


We developed a method to screen for genomic regions that exhibit loss or gain of ASM in samples from two conditions (treatments, diseases, etc.). The method relies on the availability of bisulfite sequencing data from multiple samples of the two conditions. We leverage other established computational methods to screen for these regions within a new R package called DAMEfinder. It calculates an ASM score for all CpG sites or pairs in the genome of each sample, and then quantifies the change in ASM between conditions. It then clusters nearby CpG sites with consistent change into regions. In the absence of SNP information, our method relies only on reads to quantify ASM. This novel ASM score compares favorably to current methods that also screen for ASM. Not only does it easily discern between imprinted and non-imprinted regions, but also females from males based on X chromosome inactivation. We also applied DAMEfinder to a colorectal cancer dataset and observed that colorectal cancer subtypes are distinguishable according to their ASM signature. We also re-discover known cases of loss of imprinting.


We have designed DAMEfinder to detect regions of differential ASM (DAMEs), which is a more refined definition of differential methylation, and can therefore help in breaking down the complexity of DNA methylation and its influence in development and disease.


Based on the current state of ASM detection from BS-seq reads, we set out to develop a simple yet effective method to screen for genomic regions that exhibit loss or gain of ASM between samples from distinct conditions. The methods mentioned above detect ASM in individual samples; however, they do not allow a flexible comparison between groups of samples, such as that performed in a typical differential methylation analysis [36, 37], where the goal is to find the effect of treatments or diseases on methylation, reflected as increase or decrease of methylation levels. Here, we are interested in performing such differential analysis but focusing on the effect of ASM, reflected as gain or loss of allele specificity. For this task, we introduce DAMEfinder (Differential Allele-specific MEthylation finder), an R package [38] that consists of (i) a scoring function that reflects ASM for several samples; (ii) integration with limma [39] and bumphunter [40] to detect differentially allele-specific methylated regions (DAMEs); and (iii) accurate estimation of false discovery rates (FDR). We demonstrate the ASM score and DAMEfinder on two real datasets, one based on targeted enrichment BS-seq, comparing normal colonic mucosa to cancerous colorectal lesions, and another on whole genome BS-seq (WGBS), comparing blood monocytes from healthy females and males.


The DAMEfinder pipeline. a Files necessary to run DAMEfinder are reported in yellow rectangles. White rectangles show the main R outputs from DAMEfinder. Steps to be run before DAMEfinder are in the circle, i.e., fastq files undergo quality control and read alignment with bismark [43]. The resulting bam file is used to calculate an ASM score, which can be done in two ways: b (i) the tuple-based strategy that takes as input a beforehand created methtuple [41] file. The score is calculated based on the read counts of pairs of CpG sites. (ii) the SNP-based strategy, which takes as input both the bam file and a VCF file with heterozygous SNPs. Here, the score is calculated for each CpG site in the reads containing a SNP. c We determine differential ASM by calculating a statistic based on either the tuple ASM or the SNP-ASM (using limma [39]), which reflects the difference between two conditions (Group A vs. Group B) for each genomic position (tuple or site). DAMEs are defined based on this statistic, as regions of contiguous positions with a consistent change in ASM


As depicted in Fig. 1, after calculating \(\textASM_\texttuple\) or \(\textASM_\textsnp\) in the DAMEfinder pipeline, we continue to detect regions of persistent change in ASM between one condition to another within a cohort of samples. Change can occur as loss of ASM, when a reference group exhibits allele specificity across a region (high values of ASM), and the group of interest has this same region fully methylated, unmethylated, or with random methylation (low values of ASM). Change can also occur as gain of ASM, where the reference group does not have allele specificity and the group of interest does. We call regions such as this DAMEs (Differentially Allele-specifically MEthylated regions).


We have developed a scoring method that provides a measure of allele-specific methylation, and developed a method (DAMEfinder) that detects regions that display loss or gain of allele-specific methylation, by leveraging existing methods into a single framework. We offer the possibility to detect regions exhibiting ASM based on genotype information (\(\textASM_\textsnp\)), or independent from it (\(\textASM_\texttuple\)). The latter offers a novel approach for identifying different types of ASM, such as imprinted, non-imprinted, XCI, and new types yet to be described. 041b061a72


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