Search Engine Optimization (SEO) Training Presentation

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David J. Neff, of Ridgewood : Ingenious Communication Strategies, delivered this search engin optimization workshop for the Communications and Web Teams at Best Friends Animal Society. The astute group quickly grasped how link building, site structure, alt tags, social media, and much more can improve your Google ranking.

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SEO Training No Country for Old Websites Presented by Aaron Bramley and David J. Neff @aaronmsb and @daveiam [email_address] [email_address]

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How Does Social Fit In? Fresh content drives traffic and creates inbound links

How Does Social Fit In? Fresh content drives traffic and creates inbound links • Fresh content = Blog, Flickr, YouTube

How Does Social Fit In? Fresh content drives traffic and creates inbound links • Fresh content = Blog, Flickr, YouTube • Drives traffic = Social networks

http://www.youtube.com/bestfriendsvideos http://www.flickr.com/photos/bf_photos/

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BlueGlassX - Building A Defensible Link Proﬁle by Julie Joyce

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For many small business owners, local SEO can be a confusing and overwhelming challenge on your website. In this edition Portent's monthly webinar series, you'll learn how to maximize your success as a small business against the competition in your area and industry. Portent's Director of SEO, Josh Patrice, will walk through the role local directories play, how to use social media to your advantage, the on-site factors to pay attention to, and much more. Whether you run a brick-and-mortar shop or do business through an ecommerce website, this webinar is for you. To watch the video and find other Portent webinars, visit the blog: http://www.portent.com/blog/seo/smb-seo-tips-video.htm

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Are you wondering why some people are generating new business from LinkedIn and you’re not? Join our webinar and learn how to increase targeted appointments and create new business. In this complimentary webinar, Dean DeLisle, Founder and CEO of Forward Progress, will show you the most effective methods of connecting with your targets, gaining quality appointments, and finding the potential new clients in your network. With over 350,000,000 professionals on LinkedIn, you are closer to your targeted business prospects than you think. Learn how to find them before your competitors do. You will also see what it takes to get THEM to find YOU by just using LinkedIn for less than 20 minutes a day! Forward Progress has trained over 90,000 people in over 35 countries on how to increase targeted appointments and develop more business – directly from LinkedIn! In this brief session you will learn how to: -Optimize your profile -Attract new prospects -Leverage your connections to close business -Increase targeted referrals -Gain more powerful introductions -Expand your pipeline -Find new business channels ALL registrants and attendees will receive access to the recording and materials. About Dean DeLisle: For over 30 years, Dean has demonstrated his ability to expand companies' social reach, stimulate business development through increasing engagement online, and make converting connections to new business more efficient. We’ll be seeing you online and in class!

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Content marketing is all about leads and revenue, but there are more data points along the way that can be treated as 'leading indicators' of content marketing success. Join Claye Stokes of SEO.com and David Malmborg, VP of Marketing at Right Intel as they talk about data points that most businesses are not paying attention to. Bring your content marketing strategy to the next level by registering for our next thought leader webinar. This webinar was recorded and produced by Right Intel on September 24, 2014. We appreciate SEO.com and Claye Stokes for Participating with Right Intel. You can learn more at http://rightintel.com/home/white-paper/data-points-you-should-be-tracking/

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The HPV types that cause cervical cancer are sexually transmitted, but there is little evidence that infection can be avoided by behavioural changes, such as condom use. In contrast, prophylactic vaccines against HPV infection are likely to have high efficacy. In principle, the effectiveness of HPV vaccination as a strategy for cervical cancer control can be measured either by monitoring secular trends in cervical cancer incidence or by conducting randomized trials. The former approach is unlikely to provide convincing evidence of effectiveness, since cervical cancer rates are subject to strong secular trends that are independent of intervention measures. A few phase III trials of HPV prophylactic vaccines are now being started. Such trials are very expensive studies involving frequent and complicated investigations. It is important, however, to start as soon as possible simpler trials designed to demonstrate the effectiveness of HPV vaccine in field conditions, i.e. in developing or intermediate countries which suffer the major burden of mortality from cervical cancer. Such trials may capture a difference in the most severe, and rarest, preinvasive cervical lesions (i.e., the real target of any HPV vaccine) over a prolonged follow-up (20 years at least). The design of such studies is briefly considered for two areas: Southern India and South Korea. This paper is available at: http://www.insp.mx/salud/index.html

Prospects for primary prevention of cervical cancer in developing countries

Alberto Cuadrado

Little is known about the average duration of typespecific human papillomavirus (HPV) infections and their patterns of persistence. The objectives of this study were to evaluate the rate of acquisition and clearance of specific HPV types in young women. Female university students (n 621) in Montreal were followed for 24 months at 6-month intervals. At each visit, a cervical specimen was collected. HPV DNA was detected using the MY09/MY11 PCR protocol followed by typing for 27 HPV genotypes by a line blot assay. The Kaplan-Meier technique was used to estimate the cumulative probability of acquiring or clearing a HPV infection considering types individually or in high-risk (HR) or low-risk (LR) groups defined by oncogenic potential. Incidence rates were 14.0 cases/1000 women-months (95% confidence interval, 11.4 –16.3) and 12.4 cases/1000 women-months (95% confidence interval, 10.4 –14.8) for acquiring HR and LR HPV infections, respectively. The 24-month cumulative rates of acquisition were highest for HPV-16 (12%), HPV-51, and HPV-84 (8%). Of the incident infections, HPV-16 was the most persistent (mean duration, 18.3 months), followed by HPV-31 and HPV-53 (14.6 and 14.8 months, respectively). HPV-6 and HPV-84 had the shortest mean duration time (<10 months) The mean durations of incident, same-type LR or HR HPV infections were 13.4 months and 16.3 months, respectively. Whereas the majority of episodes with a type-specific HPV infection cleared within 2 years, there were many women who were either reinfected with a new HPV genotype or presumably experienced reactivation of their initial infection.

The Natural History of Type-specific Human Papillomavirus Infections in Femal...

Alberto Cuadrado

Tibet

Marinela L

Amplification of human papillomavirus (HPV) DNA by L1 consensus primer systems (e.g., MY09/11 or GP51/61) can detect as few as 10 to 100 molecules of HPV targets from a genital sample. However, genotype determination by dot blot hybridization is laborious and requires at least 27 separate hybridizations for substantive HPV-type discrimination. A reverse blot method was developed which employs a biotin-labeled PCR product hybridized to an array of immobilized oligonucleotide probes. By the reverse blot strip analysis, genotype discrimination of multiple HPV types can be accomplished in a single hybridization and wash cycle. Twenty-seven HPV probe mixes, two control probe concentrations, and a single reference line were immobilized to 75- by 6-mm nylon strips. Each individual probe line contained a mixture of two bovine serum albuminconjugated oligonucleotide probes specific to a unique HPV genotype. The genotype spectrum discriminated on this strip includes the high-risk, or cancer-associated, HPV genotypes 16, 18, 26, 31, 33, 35, 39, 45, 51, 52, 55, 56, 58, 59, 68 (ME180), MM4 (W13B), MM7 (P291), and MM9 (P238A) and the low-risk, or non-cancerassociated, genotypes 6, 11, 40, 42, 53, 54, 57, 66, and MM8 (P155). In addition, two concentrations of b-globin probes allowed for assessment of individual specimen adequacy following amplification. We have evaluated the performance of the strip method relative to that of a previously reported dot blot format (H. M. Bauer et al., p. 132–152, in C. S. Herrington and J. O. D. McGee (ed.), Diagnostic Molecular Pathology: a Practical Approach, (1992), by testing 328 cervical swab samples collected in Digene specimen transport medium (Digene Diagnostics, Silver Spring, Md.). We show excellent agreement between the two detection formats, with 92% concordance for HPV positivity (kappa 5 0.78, P < 0.001). Nearly all of the discrepant HPV-positive samples resulted from weak signals and can be attributed to sampling error from specimens with low concentrations (<1 copy/ml) of HPV DNA. The primary advantage of the strip-based detection system is the ability to rapidly genotype HPVs present in genital samples with high sensitivity and specificity, minimizing the likelihood of misclassification.

Genotyping of 27 Human Papillomavirus Types by Using L1 Consensus PCR Product...

Alberto Cuadrado

Abstract The 18th international papillomavirus conference took place in Barcelona, Spain in July 2000. The HPV clinical workshop was jointly organised with the annual meeting of the Spanish Association of Cervical Pathology and Colposcopy. The conference included 615 abstracts describing ongoing research in epidemiology, diagnosis/screening, treatment/prognosis, immunology/human immunodeficiency virus, vaccine development/trials, transformation/progression, replication, transcription/translation, viral protein functions, and viral and host interactions. This leader summarises the highlights presented at the conference (the full text of the abstracts and lectures can be found at www.hpv2000.com). Relevant material in Spanish can be found at www.aepcc. org

Papillomavirus research update: highlights of the Barcelona HPV 2000 internat...

Alberto Cuadrado

Objectives To investigate the role of human papillomavirus (HPV) in the development of cervical neoplasia in women with no previous cervical cytological abnormalities; whether the presence of virus DNA predicts development of squamous intraepithelial lesion; and whether the risk of incident squamous intraepithelial lesions differs with repeated detection of the same HPV type versus repeated detection of different types. Design Population based prospective cohort study. Setting General population in Copenhagen, Denmark. Participants 10 758 women aged 2029 years followed up for development of cervical cytological abnormalities; 370 incident cases were detected (40 with atypical squamous cells of undetermined significance, 165 with low grade squamous intraepithelial lesions, 165 with high grade squamous intraepithelial lesions). Main outcome measures Results of cervical smear tests and cervical swabs at enrolment and at the second examination about two years later. Results Compared with women who were negative for human papillomavirus at enrolment, those with positive results had a significantly increased risk at follow up of having atypical cells (odds ratio 3.2, 95% confidence interval 1.3 to 7.9), low grade lesions (7.5, 4.8 to 11.7), or high grade lesions (25.8, 15.3 to 43.6). Similarly, women who were positive for HPV at the second examination had a strongly increased risk of low (34.3, 17.6 to 67.0) and high grade lesions (60.7, 25.5 to 144.0). For high grade lesions the risk was strongly increased if the same virus type was present at both examinations (813.0, 168.2 to 3229.2). Conclusions Infection with human papillomavirus precedes the development of low and high grade squamous intraepithelial lesions. For high grade lesions the risk is greatest in women positive for the same type of HPV on repeated testing.

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Search Engine Optimization (SEO) Training Presentation

1. SEO Training No Country for Old Websites Presented by Aaron Bramley and David J. Neff @aaronmsb and @daveiam [email_address] [email_address]

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19. How Does Social Fit In?

20. How Does Social Fit In? Fresh content drives traffic and creates inbound links

21. How Does Social Fit In? Fresh content drives traffic and creates inbound links • Fresh content = Blog, Flickr, YouTube

22. How Does Social Fit In? Fresh content drives traffic and creates inbound links • Fresh content = Blog, Flickr, YouTube • Drives traffic = Social networks

23. How Does Social Fit In? Fresh content drives traffic and creates inbound links • Fresh content = Blog, Flickr, YouTube • Drives traffic = Social networks • Inbound links = Improved ranking

24. How Does Social Fit In?

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27. http://www.youtube.com/bestfriendsvideos http://www.flickr.com/photos/bf_photos/

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Editor's Notes

Thousands of people are using this medium to talk about you in online spaces. Deal with it. Encourage it. Its a group discussion. Dive in or die.
Curative electricity was totally the Social Media of 1906. I know a lot of you are suffering from nervo-vital degrangements.
Thousands of people are using this medium to talk about you in online spaces. Deal with it. Encourage it. Its a group discussion. Dive in or die.
Thousands of people are using this medium to talk about you in online spaces. Deal with it. Encourage it. Its a group discussion. Dive in or die.
Thousands of people are using this medium to talk about you in online spaces. Deal with it. Encourage it. Its a group discussion. Dive in or die.
Thousands of people are using this medium to talk about you in online spaces. Deal with it. Encourage it. Its a group discussion. Dive in or die.
Thousands of people are using this medium to talk about you in online spaces. Deal with it. Encourage it. Its a group discussion. Dive in or die.
Thousands of people are using this medium to talk about you in online spaces. Deal with it. Encourage it. Its a group discussion. Dive in or die.
Thousands of people are using this medium to talk about you in online spaces. Deal with it. Encourage it. Its a group discussion. Dive in or die.
Thousands of people are using this medium to talk about you in online spaces. Deal with it. Encourage it. Its a group discussion. Dive in or die.
Thousands of people are using this medium to talk about you in online spaces. Deal with it. Encourage it. Its a group discussion. Dive in or die.
Thousands of people are using this medium to talk about you in online spaces. Deal with it. Encourage it. Its a group discussion. Dive in or die.
Thousands of people are using this medium to talk about you in online spaces. Deal with it. Encourage it. Its a group discussion. Dive in or die.
Thousands of people are using this medium to talk about you in online spaces. Deal with it. Encourage it. Its a group discussion. Dive in or die.
Thousands of people are using this medium to talk about you in online spaces. Deal with it. Encourage it. Its a group discussion. Dive in or die.
Thousands of people are using this medium to talk about you in online spaces. Deal with it. Encourage it. Its a group discussion. Dive in or die.
Thousands of people are using this medium to talk about you in online spaces. Deal with it. Encourage it. Its a group discussion. Dive in or die.
Thousands of people are using this medium to talk about you in online spaces. Deal with it. Encourage it. Its a group discussion. Dive in or die.

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Editor's Notes