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AWESOME ALTHOUGH I THOUGHT I WAS GETTING A FREE TRIAL BUT NOTICED I WAS CHARGED $83.88 ON 5/6/14. DISAPPOINTING BUT IF I HAVE IT FOR A YEAR? I'M OKAY BUT YOU SHOULD BE AWARE. THIS COULD BE A PROBLEM IN THE FUTURE IF IT HASN'T ALREADY. BAD BUSINESS.
2014-05-14
took a while to figure it out. Not sure if I am happy that anyone tyhat fgets a form must log into your online app. Want to have them do it in acrobat reader onlt.
2017-10-09
Pretty good. i didnt type for a long time and when i came back it blew away everything i filled out. Is there a way to keep that from happening. of course i know i can just click done but is there a way.
2018-01-18
I find it so much easier to edit documents, and save for later. Being able to share and easily find them. As well as changing page lay outs for presentations too.
2018-09-09
Still on free trial period. Have used it twice and very easy to understand.
Filled in a large medical form of 6 pages and had no hassles
As I loaded it for my home use and probably will only use it occasionally I think the cost may be unjustifiable for me to continue with it which is a pity. But it is a good product
2020-03-28
What do you like best?
The dashboard is well laid out and intuitive. It is easy to figure out the functions of buttons without referring to FAQ.
What do you dislike?
There is a little bit of a disconnect when saving your file, it's not always easy to figure where it is being saved.
Recommendations to others considering the product:
Start out with the trial. I think you will be impressed enough to purchase.
What problems are you solving with the product? What benefits have you realized?
For us it has eliminated the need to download, then print a document, fill out the blank fields, then scan it and email it to the requestor.
The dashboard is well laid out and intuitive. It is easy to figure out the functions of buttons without referring to FAQ.
What do you dislike?
There is a little bit of a disconnect when saving your file, it's not always easy to figure where it is being saved.
Recommendations to others considering the product:
Start out with the trial. I think you will be impressed enough to purchase.
What problems are you solving with the product? What benefits have you realized?
For us it has eliminated the need to download, then print a document, fill out the blank fields, then scan it and email it to the requestor.
2019-01-02
Easy to Use
Easy to Use, Excellent Editing Techniques. Loved the opportunity to email, fax and input notes. Especially loved the notification to be sent to me when my email is accessed by the recipients. GREAT SERVICE! I plan on keeping this service and using it not just for editing PDF's sent to my business, but for creating my own. THANKS PDFfiller!!! LOVE YOUR PRODUCT AND THE LOW PRICE TO USE IT.www. giftbaskets-usa. com will definitely place a link to your site on our page just for having a great service!!! No strings attached!! Respectfully,Owner of GiftBaskets-USA
2019-02-17
It has worked well. Minor issues that were easy for me to figure out. I wish there was a vertical line to assist in lining up edits needed on the documents once in pdffiller. Also it would be convenient to have an all document pagination - or if there is one, ease of finding it.
2024-01-15
A very easy to use program
A very easy to use program, though you are forced to sign up for free trial if you want to print any documents.It did what I required, so cant complain. Just would prefer it to notify of unable to print unless joined up for 30 day trial before I spent 4 hours working on translation document.
2021-04-23
Copy Number Transcript Feature
The Copy Number Transcript feature helps you understand gene expression better. This tool allows you to measure how many copies of a particular gene are present in your sample. With this information, you can make more informed decisions in your research or clinical applications.
Key Features
Quantitative measurement of gene copies
Easy integration with existing data analysis tools
User-friendly interface for efficient operation
Accurate results to enhance your research reliability
Fast processing for timely insights
Potential Use Cases and Benefits
Cancer research to track genetic variations
Genetic disorder studies to understand mutations
Pharmaceutical development for drug targeting
Agricultural biotechnology for crop improvement
Personalized medicine to tailor treatments
This feature addresses the challenge of understanding gene behavior in various contexts. By providing clear and accurate data on gene copy numbers, you gain insights that can lead to discoveries and innovations. Whether you are in a laboratory or a clinical setting, this tool aids your work and supports your goals in advancing science.
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What are copy number polymorphisms?
Copy number polymorphism: Abbreviated CNP. A normal variation in DNA due to variation in the number of copies of a sequence within the DNA. Large-scale copy number polymorphisms are common and widely distributed in the human genome.
What is meant by copy number?
copy number. The number of copies of a particular PLASMID per CHROMOSOME present in a CELL. The number of copies of a GENE in the GENOME of an ORGANISM.
What does copy number gain mean?
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 Causes copy number variation?
Copy number variants appear to be higher in brain cells than in other cell types. A likely source of copy-number variation is incorrect repair of DNA damage. Genomic duplication and replication of the gene appear to be a rare cause of Parkinson's disease, although more common than point mutations.
Is copy number variation a mutation?
These differences were named copy number variants, and they describe a segment of DNA that is 1 kilobase or larger and present at a variable copy number in comparison with a reference genome (Feud et al., 2006). Copy number variants are mutations and can include deletions, insertions, and duplications.
How many CNS are in the human genome?
About 100 CNS were detected in each genome examined with the average size being 250,000 bases (an average gene is 60,000 bases). Additional CNS will be discovered as technologies for detection improve and more DNA samples from worldwide populations are examined.
What is gene copy number?
Copy Number Variation (CNV) = En Español. 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 is a copy of a gene called?
Diploid organisms, for example, humans, have paired homologous chromosomes in their somatic cells, and these contain two copies of each gene. An organism in which the two copies of the gene are identical that is, have the same allele is called homozygous for that gene.
What does copy number mean?
The gene copy number (also “copy number variants” or CNS) is the number of copies of a particular gene in the genotype of an individual. ... For example, genes that were thought to always occur in two copies per genome have now been found to sometimes be present in one, three, or more than three copies.
What does copy number variations 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.
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