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Great product.
Good interface gives you all the options you need in one place. Clear and easy to understand. The only downside is remembering its a browser only interface, remembering the product name and having to navigate to the URL to begin. Not an issue for a daily user, but if you use only intermittently like I do, I have to make myself a reminder. To that end, I think its a little expensive for a casual user; but I do still like the interface so much that it overrides my concern on cost.
2015-12-02
I like it but felt that my "free trial" was a bit of a scam. I spent hours on a document, learning your program but was unable to print it. I don't like being "forced" into purchasing a product.
2017-05-23
I find this really easy to use. We are travelling full-time so haven't got a printer. This saves us searching for a Library or private printer to use.
2019-06-28
Besides being a great product Support is Outstanding
Besides being a great product, I would like to express how good the support is.I worked with Sam for over an hour, He went way above and beyond helping me with my Zapier Integration. Most companies would have just said that is "out of scope" Or "not my problem" Not these guys, they logged into my computer and dove deep into it and fixed my problem. Also keep in mind, I am only on a basic plan and they treated me like I was spending $1000's of dollars with them.
2020-02-04
Some functions are not readily apparent but overall it is a great tool. I had difficulty when it auto-filled a date field that I wanted to leave blank. I struggled to clear it because the dropdown appeared every time I tried, and if I deleted the current date got restored by the dropdown. Then after I finally blanked the field it jumped to another and did the same thing. Once I got that cleared it would not let me go to the next page, insisting I populate another field intentionally left blank. I used the slider to jump forward and then approach the page I wanted from the other direction.
2023-07-29
Nice experience
Nice experience, easy to understand my only dislike is the .45 cents fees that are deducted from your banking account during the free trial.
2023-07-26
I love the documents I just wish there more Tax documents to utilize. Also the first document I sent I can not find...it would have been during the trial stage ..how can I find it.
2022-02-24
Definitely recommend!!
Pdf filler was easy to use and it has endless things you can fill. I have not come across anything else like it. The team and customer service is top notch, quick, friendly and helpful!
2020-10-25
So far this program is a game changer. I wish it was cheaper (a discount for teachers on a year subscription would be wonderful!!) but I like what I am seeing so far;)
2020-08-23
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What is CNV analysis?
Introduction to CNV Analysis Copy number variations (CNS) are genomic alterations that result in an abnormal number of copies of one or more genes. Structural genomic rearrangements such as duplications, deletions, translocation, and inversions can cause CNS.
What is CNV detection?
Copy number variation (CNV) is a prevalent form of critical genetic variation that leads to an abnormal number of copies of large genomic regions in a cell. ... Correspondingly, the strong demand for NGS-based CNV analyses has fuelled development of numerous computational methods and tools for CNV detection.
What does CNV mean?
Copy number variation (CNV) is a phenomenon in which sections of the genome are repeated and the number of repeats in the genome varies between individuals in the human population.
What is CNV software?
Copy number variation detection software tools | Whole-genome sequencing data analysis. Copy number variation (CNV) is a common source of genetic variation that has been implicated in many genomic disorders. ... Usually, CNV refers to the duplication or deletion of DNA segments larger than 1 KB.
What is the difference between SNP and CNV?
A copy-number variation (CNV) or copy-number polymorphism describes variability in the number of a segment of a chromosome. It's important to remember that the scale of a CNV is larger than for an SNP.
How do CNS arise?
CNS are a type of structural variant involving alterations in the number of copies of specific regions of DNA, which can either be deleted or duplicated. ... As is the case for other types of genetic mutations, some CNS are inherited whereas others spontaneously arise de Nova.
What is CNV calling?
Abstract. Copy number variations (CNS) are gain and loss of DNA sequence of a genome. High throughput platforms such as microarrays and next generation sequencing technologies (NGS) have been applied for genome wide copy number losses.
Is copy number variation a mutation?
Copy Number Variation (CNV) A copy number variation (CNV) is when the number of copies of a particular gene varies from one individual to the next. Following the completion of the Human Genome Project, it became apparent that the genome experiences gains and losses of genetic material.
What method can be used to identify copy number variants in the genome?
Genome sequencing (GS) can be used to detect almost all classes of alleles. It is sensitive and specific for single-nucleotide variants (SNES) and indels6,7,8, and proof-of-principle studies have shown the ability to detect complex repeat expansions,9 CNS,10,11 and Vs.
What is CNV disease?
Copy Number Variation (CNV) A copy number variation (CNV) is when the number of copies of a particular gene varies from one individual to the next. Following the completion of the Human Genome Project, it became apparent that the genome experiences gains and losses of genetic material.
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